GBRAP

Genome-Based Retrieval and Analysis Parser


MAMMALIAN : Homo_sapiens_GRCh38
Assembly Assembly Locus_ID Locus_ID Version Version Definition Sequence description bp_chromo_A Total number of 'A' nucleotides in the whole sequence bp_chromo_T Total number of 'T' nucleotides in the whole sequence bp_chromo_C Total number of 'C' nucleotides in the whole sequence bp_chromo_G Total number of 'G' nucleotides in the whole sequence bp_chromo_N Total number of 'N' nucleotides in the whole sequence bp_chromo_tot Total number of nucleotides in the whole sequence fr_chromo_A Frequency of 'A' nucleotides in the whole sequence fr_chromo_T Frequency of 'T' nucleotides in the whole sequence fr_chromo_C Frequency of 'C' nucleotides in the whole sequence fr_chromo_G Frequency of 'G' nucleotides in the whole sequence fr_chromo_N Frequency of 'N' nucleotides in the whole sequence GC_chromo Percentage of ā€˜G’ + ā€˜C’ nucleotides in the whole sequence topo_entropy_chromo Topological entropy of the whole sequence chargaff_pf_chromo Chargaff's second parity rule score (method1) of the whole sequence chargaff_ct_chromo Chargaff's second parity rule score (method2) of the whole sequencee shannon_chromo Shannon entropy of the whole sequence n_gene_pos Number of genes in the positive strand n_gene_neg Number of genes in the negative strand n_gene_tot Total number of genes in the chromosome bp_gene_A Number of 'A' bases in total genes bp_gene_T Number of 'T' bases in total genes bp_gene_C Number of 'C' bases in total genes bp_gene_G Number of 'G' bases in total genes bp_gene_N Number of 'N' bases in total genes bp_gene_tot Total number of bases in total genes fr_gene_A Frequency of 'A' bases among total gene bases fr_gene_T Frequency of 'T' bases among total gene bases fr_gene_C Frequency of 'C' bases among total gene bases fr_gene_G Frequency of 'G' bases among total gene bases fr_gene_N Frequency of 'N' bases among total gene bases GC_gene Percentage of 'G' and 'C' bases in total genes topo_entropy_gene Topological entropy calculated from total gene sequences chargaff_pf_gene Chargaff's second parity rule score (method1) for total genes chargaff_ct_gene Chargaff's second parity rule score (method2)for total genes shannon_gene Shannon entropy score for total genes bp_gene_overlap_tot Number of bases overlapping between genes on two strands n_cds_pos Number of CDS in the positive strand n_cds_neg Number of CDS in the negative strand n_cds_tot Total number of CDS in the chromosome bp_cds_A Number of 'A' bases in total CDS (coding sequences) bp_cds_T Number of 'T' bases in total CDS bp_cds_C Number of 'C' bases in total CDS bp_cds_G Number of 'G' bases in total CDS bp_cds_N Number of 'N' bases in total CDS bp_cds_tot Total bases in total CDS fr_cds_A Frequency of 'A' bases among total CDS bases fr_cds_T Frequency of 'T' bases among total CDS bases fr_cds_C Frequency of 'C' bases among total CDS bases fr_cds_G Frequency of 'G' bases among total CDS bases fr_cds_N Frequency of 'N' bases among total CDS bases GC_cds Percentage of 'G' and 'C' bases in total CDS topo_entropy_cds Topological entropy calculated from total CDS sequences chargaff_pf_cds Chargaff's second parity rule score (method1) for total CDS chargaff_ct_cds Chargaff's second parity rule score (method2) for total CDS shannon_cds Shannon entropy score for total CDS bp_cds_overlap_tot Number of bases overlapping between CDS on two strands bp_cds_intron_A Number of 'A' bases in total introns between CDS bp_cds_intron_T Number of 'T' bases in total introns between CDS bp_cds_intron_C Number of 'C' bases in total introns between CDS bp_cds_intron_G Number of 'G' bases in total introns between CDS bp_cds_intron_N Number of 'N' bases in total introns between CDS bp_cds_intron_tot Total bases in total introns between CDS fr_cds_intron_A Frequency of 'A' bases in total introns between CDS fr_cds_intron_T Frequency of 'T' bases in total introns between CDS fr_cds_intron_C Frequency of 'C' bases in total introns between CDS fr_cds_intron_G Frequency of 'G' bases in total introns between CDS fr_cds_intron_N Frequency of 'N' bases in total introns between CDS GC_cds_intron Percentage of 'G' and 'C' bases in total introns between CDS topo_entropy_cds_intron Topological entropy calculated from total intron sequences between CDS chargaff_pf_cds_intron Chargaff's second parity rule score (method1) for total introns between CDS chargaff_ct_cds_intron Chargaff's second parity rule score (method2) for total introns between CDS shannon_cds_intron Shannon entropy score for total introns between CDS bp_cds_intron_overlap_tot Number of bases overlapping between introns between CDS on two strands n_ncRNA_pos Number of ncRNA in the positive strand n_ncRNA_neg Number of ncRNA in the negative strand n_ncRNA_tot Total number of ncRNA in the chromosome bp_ncRNA_A Number of 'A' bases in total ncRNA bp_ncRNA_T bp_ncRNA_T bp_ncRNA_C Number of 'C' bases in total ncRNA bp_ncRNA_G Number of 'G' bases in total ncRNA bp_ncRNA_N Number of 'N' bases in total ncRNA bp_ncRNA_tot Total bases in total ncRNA fr_ncRNA_A Frequency of 'A' bases among total ncRNA bases fr_ncRNA_T Frequency of 'T' bases among total ncRNA bases fr_ncRNA_C Frequency of 'C' bases among total ncRNA bases fr_ncRNA_G Frequency of 'G' bases among total ncRNA bases fr_ncRNA_N Frequency of 'N' bases among total ncRNA bases GC_ncRNA Percentage of 'G' and 'C' bases in total ncRNA topo_entropy_ncRNA Topological entropy calculated from total ncRNA sequences chargaff_pf_ncRNA Chargaff's second parity rule score (method1) for total ncRNA chargaff_ct_ncRNA Chargaff's second parity rule score (method2) for total ncRNA shannon_ncRNA Shannon entropy score for total ncRNA bp_ncRNA_overlap_tot Number of bases overlapping between ncRNA on two strands bp_nc_intron_A Number of 'A' bases in total introns between ncRNA bp_nc_intron_T Number of 'T' bases in total introns between ncRNA bp_nc_intron_C Number of 'C' bases in total introns between ncRNA bp_nc_intron_G Number of 'G' bases in total introns between ncRNA bp_nc_intron_N Number of 'N' bases in total introns between ncRNA bp_nc_intron_tot Total bases in total introns between ncRNA fr_nc_intron_A Frequency of 'A' bases in total introns between ncRNA fr_nc_intron_T Frequency of 'T' bases in total introns between ncRNA fr_nc_intron_C Frequency of 'C' bases in total introns between ncRNA fr_nc_intron_G Frequency of 'G' bases in total introns between ncRNA fr_nc_intron_N Frequency of 'N' bases in total introns between ncRNA GC_nc_intron Percentage of 'G' and 'C' bases in total introns between ncRNA topo_entropy_nc_intron Topological entropy calculated from total intron sequences between ncRNA chargaff_pf_nc_intron Chargaff's second parity rule score (method1) for total introns between ncRNA chargaff_ct_nc_intron Chargaff's second parity rule score (method2) for total introns between ncRNA shannon_nc_intron Shannon entropy score for total introns between ncRNA bp_nc_intron_overlap_tot Number of bases overlapping between introns between ncRNA on two strands n_tRNA_pos Number of tRNA in the positive strand n_tRNA_neg Number of tRNA in the negative strand n_tRNA_tot Total number of tRNA in the chromosome bp_tRNA_A Number of 'A' bases in total tRNA bp_tRNA_T Number of 'T' bases in total tRNA bp_tRNA_C Number of 'C' bases in total tRNA bp_tRNA_G Number of 'G' bases in total tRNA bp_tRNA_N Number of 'N' bases in total tRNA bp_tRNA_tot Total bases in total tRNA fr_tRNA_A Frequency of 'A' bases among total tRNA bases fr_tRNA_T Frequency of 'T' bases among total tRNA bases fr_tRNA_C Frequency of 'C' bases among total tRNA bases fr_tRNA_G Frequency of 'G' bases among total tRNA bases fr_tRNA_N Frequency of 'N' bases among total tRNA bases GC_tRNA Percentage of 'G' and 'C' bases in total tRNA topo_entropy_tRNA Topological entropy calculated from total tRNA sequences chargaff_pf_tRNA Chargaff's second parity rule score (method1) for total tRNA chargaff_ct_tRNA Chargaff's second parity rule score (method2) for total tRNA shannon_tRNA Shannon entropy score for total tRNA bp_tRNA_overlap_tot Number of bases overlapping between tRNA on two strands n_rRNA_pos Number of rRNA in the positive strand n_rRNA_neg Number of rRNA in the negative strand n_rRNA_tot Total number of rRNA in the chromosome bp_rRNA_A Number of 'A' bases in total rRNA bp_rRNA_T Number of 'T' bases in total rRNA bp_rRNA_C Number of 'C' bases in total rRNA bp_rRNA_G Number of 'G' bases in total rRNA bp_rRNA_N Number of 'N' bases in total rRNA bp_rRNA_tot Total bases in total rRNA fr_rRNA_A Frequency of 'A' bases among total rRNA bases fr_rRNA_T Frequency of 'T' bases among total rRNA bases fr_rRNA_C Frequency of 'C' bases among total rRNA bases fr_rRNA_G Frequency of 'G' bases among total rRNA bases fr_rRNA_N Frequency of 'N' bases among total rRNA bases GC_rRNA Percentage of 'G' and 'C' bases in total rRNA topo_entropy_rRNA Topological entropy calculated from total rRNA sequences chargaff_pf_rRNA Chargaff's second parity rule score (method1) for total rRNA chargaff_ct_rRNA Chargaff's second parity rule score (method2) total rRNA shannon_rRNA Shannon entropy score for total rRNA bp_rRNA_overlap_tot Number of bases overlapping between rRNA on two strands ATG ATG AAG AAG GTA GTA ACT ACT GCA GCA GAG GAG GCT GCT ATT ATT TCC TCC TGG TGG AAT AAT GAA GAA TCA TCA ACG ACG AGT AGT AAC AAC TCT TCT GTG GTG TTC TTC TTT TTT CTG CTG GGT GGT CTC CTC GAT GAT CAG CAG ACC ACC CTA CTA TTG TTG TAT TAT GGA GGA ATC ATC CTT CTT GTC GTC ATA ATA ACA ACA GAC GAC CAC CAC CCC CCC TAC TAC GCC GCC AGC AGC CGC CGC AAA AAA GGC GGC TGC TGC GTT GTT GGG GGG AGA AGA TGT TGT CAT CAT TCG TCG GCG GCG TTA TTA CCT CCT AGG AGG CCA CCA TAG TAG CGG CGG CCG CCG CGT CGT CAA CAA TAA TAA TGA TGA CGA CGA
GCF_000001405.40NC_000001NC_000001.11Homo sapiens chromosome 1; GRCh38.p14 Primary Assembly.67070277672441644805504348111528184754082489564200.270.270.190.190.070.390.77280.00190.99811.936220082032404040701222437931523014893031259173935091459959860.260.280.230.2300.460.91850.0980.91011.9754417591105210102062868656741884887513902089034001420.270.220.250.2600.510.86160.31290.75021.938432255848324922315166328981741703093509816242350.250.290.220.2300.460.89470.19080.83671.949909329591891933332902014774906770855033811070.280.240.240.2400.480.87260.27470.77751.94871778122468074143540140754689190267567150.270.290.220.2200.440.90290.16150.86041.960404043831034141516482001060980.170.230.270.3300.60.87370.26790.77151.9529001717374458562663020570.180.220.270.3200.60.87470.18340.83221.96760252753056177481544520950315272172814661211942402714562264451914173601497016065185842437219473154433856411395215011636137253199541013316276102142443717183164841300289931986818817175002417011772279372317599762411722697193791098219182231181442314890597493999265229922100125935498311430104825482184295740167126520
GCF_000001405.40NC_000002NC_000002.12Homo sapiens chromosome 2; GRCh38.p14 Primary Assembly.7179121371987932483181804845090316452922421935200.30.30.20.20.010.40.63090.00270.99731.9686149614912987429372264608452729631717307140262683911496358870.270.290.220.2200.440.92060.09310.91461.97186923547076151322684367571079601447625840024827330.280.230.230.2500.480.8630.31030.7511.93970217915012401652515000520157050150765135610.270.310.20.2100.420.89680.1760.84791.94188447880286616681016970999983774884778994035708310.280.250.230.2400.470.87310.270.78061.94879973393610084641645818265722350328489940.280.30.210.2100.420.90440.14590.87241.95654998453810414014718805790.190.250.250.3200.570.86550.31240.73881.95780000000000NANANANANANANANANANA01995824086665411509152192108514289129041332816343137062237014763498111349130551319717286140251371526174824914693141462462912839779514040881115800124371289690689005155521358711915142789025171361564461882316214027129909382114621809710524113354348626888621535113614176424399670965883658149815891119114519
GCF_000001405.40NC_000003NC_000003.12Homo sapiens chromosome 3; GRCh38.p14 Primary Assembly.596890915983330239233483393442591954171982955520.30.30.20.200.40.66670.00260.99741.96841194111823123663485239284656250225112591849021268605110.280.290.210.2200.430.92180.08950.9171.97071568285475451092518527441514485553493674019392680.280.230.240.2600.490.86410.3060.75391.94140193286142122106413314017139336362677973330.260.30.210.2300.440.89690.17620.8481.948106605871247805069788790582524586144027625270.290.260.220.2300.460.87250.2740.77741.94673578766648171567511015152006310263590130.290.30.20.2100.410.90520.14140.87611.9527749291346365719102900.220.220.240.3100.560.89080.15450.86181.98240000000000NANANANANANANANANANA01483317468504289861224717177117789357108921311498641651411381389584841011410042142641157710613212156158118951033520626106506050100226757125391034510157760160621222210774969711863716514047124884859159511162810573692393061374384529194328046156000125071055114465310355855083287611299395792853568
GCF_000001405.40NC_000004NC_000004.12Homo sapiens chromosome 4; GRCh38.p14 Primary Assembly.585612365862343036236976363310254618881902145550.310.310.190.1900.380.94480.00180.99821.958595691118673110224633167310199766902063216901048784150.290.30.20.2100.410.92160.08570.92071.9604422470406388794382760318668311856329307013425910.290.250.220.2400.460.86430.3090.75211.937312115078226164727539694866101227510513685960.290.320.190.200.390.90160.1510.8671.93505725301102625550604054437731445203021125380.30.260.220.2300.440.87230.27240.77791.9443985998778879707529199753442850281158660.30.310.190.200.390.90570.13490.88141.94454118011151618230720.210.220.250.3200.570.8870.15420.86011.97960000000000NANANANANANANANANANA0105371263938866655807211181762077556842843184101311477352456661175337225898575738554125584237754680691297467174234761653828760690673905068537286657458642466524921809680832767134906959661954415573101916231665522943155555277116984883323973375332118768640337565442416
GCF_000001405.40NC_000005NC_000005.10Homo sapiens chromosome 5; GRCh38.p14 Primary Assembly.546990945495501035731600358796742728811815382590.30.30.20.200.390.94380.00440.99561.96721045101220572954428331625615200808812076417020001020169490.280.290.210.2200.430.92130.09170.91561.9689459551490411901414952349262377505392332015340510.280.230.230.2500.480.86430.31080.75091.9394014044576154627349665276100944871000492680730.270.310.20.2100.420.90010.16150.85861.944905525881140610998600579467396465492021444650.290.250.230.2300.460.8720.27450.77741.9466079152708185888509686651877330263857570.290.30.210.2100.410.90550.13980.87731.95354270181018255295366431013470.190.220.270.3200.590.88030.17360.84681.96470000000000NANANANANANANANANANA0112891381741467125905314203896077738680957787641362286863289674683678256120379075845816298484787349058151828383474481255432977781317579593852769485959471429078588311123994540691329292427484568370881096963836621306547235120940182501055823744500445421868603324670922826
GCF_000001405.40NC_000006NC_000006.12Homo sapiens chromosome 6; GRCh38.p14 Primary Assembly.513454775137302533646690337133307274561708059780.30.30.20.200.390.85220.00130.99871.96631210117323832968734131714458200420702075364701021975160.270.280.220.2300.450.9190.09920.90911.97163854395275361063458848385364429210441664017150860.280.230.240.2600.490.86370.30870.75221.93990151082341655493010066147105337830522630940.270.30.210.2200.430.89580.19260.83661.944106115741185724617707401536423539728025081690.280.250.230.2300.460.87430.26650.78291.9498569231107166639451550745903920231956480.280.30.210.2100.420.90340.15550.86571.953629028757915422862614290736820114890.20.230.250.3200.570.8860.23110.79971.9670000000000NANANANANANANANANANA012957159994380810310319153191049185289955117978453148809894369676398618929911810933891171844556511026689121800396595338897458531135789678746652054901033691738297110755937124881131544931441410326881460398940126037280756430154743535611172100031268328265169498624659723363480753234
GCF_000001405.40NC_000007NC_000007.14Homo sapiens chromosome 7; GRCh38.p14 Primary Assembly.470582484721504032317984323788593758381593459690.30.30.20.200.410.71230.00260.99741.9736110498420882780202029935989196522372034145052396977840920.270.280.220.2300.450.91920.09890.90981.9708171388479473952411053350119416813410330015883150.270.230.250.2600.510.86250.30790.75261.9379691645412118162645116066331214468752396584204820.260.290.220.2300.450.89750.17780.8471.947605535051058654701641897488857493313022787680.280.250.230.2400.470.87210.27370.77751.9461053965475572126358297736302890181819390.280.30.210.2200.430.90330.15420.86581.955210911813922349353381500015830.220.220.240.3200.560.88480.17110.84941.98010000000000NANANANANANANANANANA01103713405386272831006513706977671739560109927752128039077369666497908806611525897482041769849829913774016096888848497660509310169787979096154496297868628834011484568012556109785014120671002585585435821311090666269313180509447681113192911264619545513543425489406277768783251
GCF_000001405.40NC_000008NC_000008.11Homo sapiens chromosome 8; GRCh38.p14 Primary Assembly.433335304330064629030173291037873705001451386360.30.30.20.200.40.94560.00160.99841.97058298861715246674292643937617031262176220060857600730.270.290.220.2200.440.920.09010.91681.968997212340384724305365256802297415307420011670020.280.230.240.2600.490.8630.30720.75331.935801242401313646181850515788865270434618780.260.30.210.2200.440.89710.17140.85211.93930488510998572612562236444393442420020216610.280.250.230.2400.470.87290.2750.77691.94791262661496488167417607542432190211736100.280.30.210.2100.420.90550.14750.87131.9548032575859212203740.20.230.240.3300.570.86660.24640.79111.96880000000000NANANANANANANANANANA086781059527945069727810993694754336531772556549539615227274938581258558711652360431295636387002572412495644333375866371375355915571945443667690966545955773641449413799037089256758264974056604584084965492622013872364074346813833918754182390818336260250552852100
GCF_000001405.40NC_000009NC_000009.12Homo sapiens chromosome 9; GRCh38.p14 Primary Assembly.35736329357837482509981125170662166041641383947140.260.260.180.180.120.360.77150.00210.99791.90298438871730201898182184849014959514155125403196725135580.260.270.230.2300.460.9190.0940.91351.9722271495372408780343521290342361721361956013575400.260.220.250.2700.520.8620.30540.75421.93650972358610862669746010578389170358852770.240.280.230.2400.470.89510.18530.84081.94970472477949582271572276462507465817020828710.280.250.230.2400.480.87250.27610.77641.9466183645498234770088312804431863873196156375380.270.290.220.2200.430.90190.15540.86541.95631352310222837354501450.20.260.230.3100.550.83010.27590.76141.97730000000000NANANANANANANANANANA0971911628306359258473128248291555983099302600810698749932165563661468591021976796152154484496882566321453581763580607038139133720664245619326280098171719299854878119509778432895639368761242557648926456955871263143423433944578921012018034886479522707165223261282809
GCF_000001405.40NC_000010NC_000010.11Homo sapiens chromosome 10; GRCh38.p14 Primary Assembly.388759263902755527639505277199765344241337973860.290.290.210.2100.410.57810.00340.99661.977187083917092324309025205924170335401770497390001832775280.270.280.220.2300.450.92120.09170.91521.975794394401360761353520288805330377340078013127800.280.230.240.2600.490.86420.30970.75151.9396013207795147433489709779102016831478626060.260.30.210.2200.440.90050.16540.85561.953723428490485975537983529366442609440152019501100.280.250.240.2400.480.87440.2660.78251.953669743449164467881305377830829690149495440.280.290.210.2200.430.90360.15470.86551.960386751234353607302290.190.230.260.3200.580.88880.20180.82061.96510000000000NANANANANANANANANANA09970121163197603082121169879256218750588726812115337436301656526787679793526993653713577416776907107131897341391366354112880965556408500540648202746366948554452896958620353211433807470154598681197535527579224333859402085187558993620624203415319897613265561992636
GCF_000001405.40NC_000011NC_000011.10Homo sapiens chromosome 11; GRCh38.p14 Primary Assembly.392867303936195427903257279818015528801350866220.290.290.210.2100.410.94490.00240.99761.97711651119228423044322246722101721211017800423124694828537590.260.270.230.2400.470.91820.1030.90611.97392697716686351303479799436129541480522825019802330.250.220.260.2700.530.86150.30640.75341.9387118116622131281804387929219190673100000425638500.240.270.240.2500.490.88860.20710.82511.94560495479974499547484788409702413821018078580.270.240.240.2500.480.87030.28410.77181.9457045321064683051312004231747930155099920.270.290.220.2200.440.90280.15610.86451.960760251761319524023030209670.20.250.240.3100.550.87910.2560.77931.97520000000000NANANANANANANANANANA01506015959441090611246218246128118590127401395378651310310556453977569332103141570512184931624769624613944924220436121505968928460961242011273961183764873111641132310778157337407175621366465101192713920120586011113921196986098325352058544707140321129216039246072286443307910188281683783971
GCF_000001405.40NC_000012NC_000012.12Homo sapiens chromosome 12; GRCh38.p14 Primary Assembly.393701093949222527092804271826781374901332753060.30.30.20.200.410.77220.00320.99681.9747102110402061243868362610313217392472179665622102858511040.270.280.220.2200.450.92030.09190.91531.97361332295245161040461135393430443961452163017506890.270.230.240.2600.50.86310.31120.75041.940501282170014111379920842996205932102457642030.260.30.220.2300.440.89490.19140.83641.949905095291038526934508900414296411869018619990.280.250.230.2400.470.87270.27970.7741.947429251523915273737348830235264710174409010.280.290.210.2200.430.90380.14960.86991.95811410854911614917521906590.180.230.270.3300.60.89080.23950.7911.95770000000000NANANANANANANANANANA0132631618144268146104941674610792852610161118838838146419592362374379377910312821101499258197695577113139112183949803537188525920113229708883471085256100689859891511872637813179117844613138501077491316061888711961753976682998446552671114196371242625115726479127139771331479763401
GCF_000001405.40NC_000013NC_000013.11Homo sapiens chromosome 13; GRCh38.p14 Primary Assembly.30047611301627171883919218933605163812001143643250.260.260.160.170.140.330.77160.00440.99561.87195125231035149005781585865897233141009895150000506315010.290.30.20.2100.410.92090.08910.91771.964216412217217534717747414656014709815355606246880.290.240.220.2400.460.86410.30750.75291.93690771870984590125074400533403350000266361540.280.320.190.200.40.90350.15520.8631.94220347347694328074318606237185242560011264250.290.260.220.2300.450.87180.27430.77691.9456044331344519643274669727825610144820350.290.310.20.200.40.90540.13740.87971.9472166600445072759402910.170.250.260.3200.580.88830.30050.75181.95710000000000NANANANANANANANANANA0472359791676289435875103334836293440364237835964350613452847359933164045383739715884189435293535619730851971343525074006335133222399242939943405297732122443381839511428664536113072253127714853286829121159171423823517322439561174161218309183730171529611096
GCF_000001405.40NC_000014NC_000014.9Homo sapiens chromosome 14; GRCh38.p14 Primary Assembly.26673415269119431842375818559033164755691070437180.250.250.170.170.150.350.94410.00810.99191.87558487291577161837081745539911553451119813680571739260.270.280.220.2300.450.9190.10060.90811.97395302315293608270235228866262059270717010318770.280.230.240.2600.490.86370.31230.74971.9375073948128257069533799856093300265992090.260.30.220.2300.440.89490.18820.83871.94720409340749376652368958303712304523013538450.280.250.230.2400.470.87150.27770.77591.946138034373983770245950025005820127472890.280.30.210.2100.420.90450.15360.86651.9538010919248326349478014010.180.240.250.3400.580.88020.28910.75761.9570000000000NANANANANANANANANANA07628964226124776639410423638947165811665649529210541622064396525754547720582453371192532876293595810584568631755249348863835242520339473125589161575135679237658254696630498056648454623594535770184220443319662964308967395878756914083555298615735435178543492000
GCF_000001405.40NC_000015NC_000015.10Homo sapiens chromosome 15; GRCh38.p14 Primary Assembly.24508669245538121775294117825903173498641019911890.240.240.170.170.170.350.94460.0030.9971.86787466371383158370681707238111771681122311473569122800.270.280.220.2300.450.92050.09590.91171.9777147760291312603308576252598295653311497011683240.280.220.240.2600.50.86110.31720.7471.9392081960669098437609743263883533297802910.250.290.220.2300.450.89630.1830.84211.95470444326770411122399185325476329093014648760.270.250.240.2400.480.87350.27480.77781.948260431731573277309226712923039630110215580.270.290.220.2200.440.90440.1610.85931.9623244245911815917321106610.180.240.260.3200.580.89910.2470.78511.96430000000000NANANANANANANANANANA086171090626835134744412559718149886652830152539961658024835159582759778406619154711318136776971614913106644333685683359676015786559943983341705667335818756839469014844831588966742064743743601683784981523121503196332176487561851617783847344117366535211356392303
GCF_000001405.40NC_000016NC_000016.10Homo sapiens chromosome 16; GRCh38.p14 Primary Assembly.225583192277490618172742182999768532401903383440.250.250.20.20.090.40.85250.00830.99181.9338237791602129690781400128711160842115212390496524460.240.250.250.2500.50.91560.10280.9061.97665761474391865327364281906410021403101014223920.240.210.270.2800.560.86040.29730.75961.9367075918548439115656170368534490294461210.220.260.260.2700.520.8860.21570.81891.94750358371729319278309342296909291487012170160.260.230.250.2500.50.87170.26990.78061.947512469829256070018063771830934086678400.260.280.230.2300.460.8980.17260.85251.960151126313437511659019200.160.230.270.3400.610.88780.2940.75021.94550000000000NANANANANANANANANANA09031113152541580591661483195394107900910347447389297444408951216541669711578762749841825245809632605815869892533295436273893387001599560092609779589978253131264633142051089959747096114148969383495538770554456653290608124391100192131142313907005643429706277160057213196
GCF_000001405.40NC_000017NC_000017.11Homo sapiens chromosome 17; GRCh38.p14 Primary Assembly.22639499227052611872394418851500337225832574290.270.270.220.2300.450.63090.00480.99521.991497710932070139470081507927412289985126920270540082940.240.260.250.2500.50.91540.10340.9061.98072169485476341181462598394607546922543029019471560.250.210.270.2800.540.86190.30680.75271.9391082025089129741710338274222420318578730.230.260.250.2600.510.88590.21660.81751.95120440441881337157327378326533320329013113970.260.230.250.2600.510.87170.27180.77981.9497561996769207145816243841650300073429110.250.270.240.2400.480.89850.17430.85111.966841907161733463549625795024320.190.230.260.3300.580.88540.22260.80411.96580000000000NANANANANANANANANANA01287016667375777661218621430129696386127441390163681342396954942715394059264150311074072142503565051321886342207712703495875764645126911043583578024376210202125731066116850696918539149977409105851506312897539112319117567874768941966835365213654119011495220358590742334469455253482424437
GCF_000001405.40NC_000018NC_000018.10Homo sapiens chromosome 18; GRCh38.p14 Primary Assembly.24050680241828191579445516061651283680803732850.30.30.20.200.40.94390.01110.9891.967738939978812029991129013728289724856366750000418347540.280.30.210.2100.420.9220.09030.91661.96973399215113228314807812135412745513254405294310.290.240.220.2400.470.86560.30010.75721.94210622450868718874314697451368150000219747730.280.320.190.200.40.90550.15050.8671.9473024827051828058126884321616221691309824990.290.250.230.2300.460.87540.26650.78191.949402944876304642119289401941443098616800.290.30.210.2100.410.90540.14510.87331.955295829011141717250730.190.230.230.3400.580.90440.28730.75181.96550000000000NANANANANANANANANANA04170486115112517324645222994277828683227304951113184115025103042288436762997298149731689287731085041265016422911193432972676276219491942351429522712284518483368343414035035304526412137228739892326253899714811947311529183753790154216017783220114624601080
GCF_000001405.40NC_000019NC_000019.10Homo sapiens chromosome 19; GRCh38.p14 Primary Assembly.15142293152827531395458014061132176858586176160.260.260.240.2400.480.94010.00840.99161.997110881005209391964699967819930464095252390379941670.230.250.260.2600.520.91380.10780.90211.98022293926906971387508170426057659178635753022291580.220.190.290.2900.590.85740.320.74551.9214047064545276871490041150810660199648020.20.230.280.2900.560.87650.26960.78041.9388037830468221644420608721236420827808431730.250.230.260.2700.530.86870.28370.77181.94501215573128118310772611081537046555540.250.270.240.2400.490.89520.19740.83341.964510023034710012613616505270.190.240.260.3100.570.88040.2250.80211.97360000000000NANANANANANANANANANA0148881754345807880138502324614096483014653165828143116861170370628186115049377207651340359742913666691462768322284615892517075053618143181148589199313583213073137101338322362708823756170751097993301874413000423015421149897131768954741078748891792814876174331954114591126341838777293689454926
GCF_000001405.40NC_000020NC_000020.11Homo sapiens chromosome 20; GRCh38.p14 Primary Assembly.17867246180664061391613314094472499910644441670.280.280.220.220.010.430.94530.01190.98821.9846583534111795814091033803379228208178489406360211570.250.260.240.2400.480.91990.09220.91481.98064896528925254119328616028122567722544808046920.250.210.260.2700.540.86170.30950.75131.9356054178975960639440696645956770203811790.230.270.240.2500.50.89360.18960.83781.95630301278579296774292364265386262298011168220.260.240.250.2500.510.87470.25910.78721.9533218030461880858141670414327285865333940.260.280.230.2400.470.89950.16890.85541.963611029000000000NANANANANANANANANANA0000000000NANANANANANANANANANA0553071831493329352638257523525575044580728415425416023503077385635096252422130499818261152063530874250711942320018145282410334013373165443365109451867822785795364013189466064334983220448525005306031061906334415045557537764668633524348313483816101533341767
GCF_000001405.40NC_000021NC_000021.9Homo sapiens chromosome 21; GRCh38.p14 Primary Assembly.1182066411856330818524482263816621361467099800.250.250.180.180.140.350.77090.0040.9961.88533093076165657701608201242537174397908100021204913590.260.270.230.2300.470.91370.11390.89731.96821121871151332488720675459910989294903467120.260.220.250.2700.520.86090.31820.74631.930302310658257128918281741907288086174090.240.280.230.2400.470.89760.17950.84461.9515019117636719195518808516700516760807146530.270.250.240.2500.490.87190.25780.78941.9466017259131787632114222911645662058203600.270.290.220.2200.440.90180.15750.8631.95390011101521250710.140.210.30.3500.650.88090.2870.75331.92220120124808621814204147441399750.120.160.360.3700.720.8720.14650.86831.846202326293872514552006294220221378238424201416260019501035153716591889265418531663378511491937148836332115816162211532487163414941383886198119331763242812662664271610592581242730261069190025101752131176811709562277204226445161198129561617646321641667
GCF_000001405.40NC_000022NC_000022.11Homo sapiens chromosome 22; GRCh38.p14 Primary Assembly.10382214103707259160652924618611658686508184630.20.20.180.180.230.360.71170.00520.99481.8289466424890617050367308845879304608562950000249163200.240.250.250.2600.510.91760.0980.90971.98256341523821745515634613224620472520069906940160.240.20.280.2900.570.85990.30050.75761.9359033671063772512319819133413640136791730.210.250.260.2800.540.88910.19860.83141.9554019620640218101717844818670318735607335240.250.230.260.2700.520.86960.27570.77751.950409268879892118121368239315000036021650.240.270.240.2500.490.89450.17990.84661.96390101162519240840.190.30.230.2900.510.8870.33580.71581.97750000000000NANANANANANANANANANA0450557541120271646717563481017894635513317684079332522792408314630695726371021459268226546662680793646431686230113234664342425832851979347947854034649924187325560932612942604044071655458938902430271818133089893517746595700614335834331325306565129561665
GCF_000001405.40NC_000023NC_000023.11Homo sapiens chromosome X; GRCh38.p14 Primary Assembly.4675480746916701305237803069774111478611560408900.30.30.20.20.010.390.66670.00460.99541.9642718683140118368275199768681271767913058794280000644016160.270.280.220.2300.450.91770.11020.91.9697253444438390828337051279881320917330406012682550.280.230.240.2600.50.86460.31170.74991.9438495161031055293865558316762651180000335675230.260.30.220.2200.440.89490.19610.83371.9456026528254728032527834621184720935709798750.280.260.230.2400.460.8710.28350.77221.9454032796823464580215812421929360110953220.280.30.210.2100.430.90390.16940.85571.955500445758849602950.190.20.280.3300.610.91790.12430.8841.95570000000000NANANANANANANANANANA010343119353277595580241330477485963727579456315111837008248956946616684392037154634913591452076157343131277168397561974197836365006073505638807077710061758064465410316847734699963804563184305645386354879551022333232366985837236980817353681368219797388211354762415
GCF_000001405.40NC_000024NC_000024.10Homo sapiens chromosome Y; GRCh38.p14 Primary Assembly.788619279561685285789528689430812367572274100.140.140.090.090.540.180.66660.00450.99551.4246100911911490896165875510862281109275053451540.270.290.220.2200.440.91290.12820.88451.96730402565236772041421686231100888870.280.240.230.2500.480.86870.31440.75031.94060478513575190369308380507018035180.270.320.20.2100.410.88780.21290.81851.928059661255288651508434664227201901320.270.250.240.2400.480.86860.24690.79431.9621135449617482877322942326305015817410.270.30.210.2200.440.8970.18560.84181.95960000000000NANANANANANANANANANA0000000000NANANANANANANANANANA0730848293488592953556427461565545671586227352401446747548489902309435446978513272428414561478393348314541464403437307665515262648494417360409604360346209237310588439674194322259131459138396180
NANC_012920NC_012920.1Homo sapiens mitochondrion; complete genome.51244094518121691165690.310.250.310.1300.440.9260.52150.60881.93042893746323985456022381154160.310.290.230.1700.410.87320.44590.66331.907855516108810841105659039360.290.280.280.1600.440.87520.62220.57291.885846000000NANANANANANANANANANA0000000000NANANANANANANANANANA0000000NANANANANANANANANANA014822479456275298015080.320.30.180.200.380.86530.36620.70411.91011202862549650451125130.340.220.260.1800.440.90410.39780.66881.9596023438182315235021415222234351716432917173482388411203361202557392327433137962528616201384725151152225222279