chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124898299748982998AC10GENIChomozygous50230548
124898331148983312CCT15GENICheterozygous50230550
124898331148983312CCTTT15GENICheterozygous50559364
124898337648983377AG15GENIChomozygous50230552
124898362048983621TTC29GENIChomozygous50230554
124898386648983867GA38GENIChomozygous50230556
124898437448984375CT39GENIChomozygous50230558
124898553248985533GA62GENIChomozygous50230560
124898564748985648AATG71GENIChomozygous50230562
124898569848985699TC74GENIChomozygous50230564
124898597448985975AG33GENIChomozygous50230566
124898605348986054AC24GENIChomozygous50230568
124898616648986167AG21GENIChomozygous50230570
124898646748986468TG10GENIChomozygous50230572
124898652748986528TC14GENIChomozygous50230574
124898670348986704TG24GENIChomozygous50230576
124898670548986706AG24GENIChomozygous50230577
124898680848986809GGT21GENIChomozygous50230579
124898717848987179CT24GENIChomozygous50230581
124898725948987260CT28GENIChomozygous50230583
124898728748987288AG27GENIChomozygous50230585
124898729348987294AG26GENIChomozygous50230587
124898776748987768CG22GENIChomozygous50230589
124898854048988554GTGTGTGTGTGTGT--------------10GENIChomozygous50575602
124898884248988843CA19GENIChomozygous50230593
124898888848988889AAT18GENICheterozygous50230595
124898888848988889AATT18GENICheterozygous50230597
124898899648988997GGAA8GENICheterozygous50230599
124898899648988997GGAAA8GENICheterozygous50575604
124898950348989504CT31GENIChomozygous50230601
124898961748989618GA30GENIChomozygous50230603
124898974248989743AAC24GENIChomozygous50230605
124899028948990290TC21GENIChomozygous50230607
124899057348990574AG28GENIChomozygous50230609
124899238548992386AG33GENIChomozygous50230611
124899326048993261CG33GENIChomozygous50230613
124899362148993622TC24GENICpossibly homozygous50230615
124899396448993965CCGTGT9GENICheterozygous50230619
124899558648995587AG20GENIChomozygous50230621
124899559548995596TA22GENIChomozygous50230623
124899600448996005GC22GENIChomozygous50230624
124899679648996797AG20GENIChomozygous50230626
124899692248996925TTT---6GENICheterozygous50230628
124899749848997499GT35GENIChomozygous50230632
124899781248997813GT35GENIChomozygous50230634
124899808448998085AG17GENIChomozygous50230636
124899813848998139C-23GENIChomozygous50230638
124899814348998144GA21GENIChomozygous50230640
124899822548998226GGT21GENIChomozygous50230642
124899876248998763TA37GENIChomozygous50230644
124900011249000113TC44GENIChomozygous50230646
124900065249000653GA20GENIChomozygous50230648
124900076749000768AAAAAC16GENIChomozygous50230650
124900080249000803GA31GENIChomozygous50230652
124900099449000995TC42GENIChomozygous50230654
124900113249001133CCG6GENICheterozygous50230656
124900114449001145GGT14GENIChomozygous50230658
124900143449001435CG21GENIChomozygous50230660
124900174049001741CT30GENIChomozygous50230662
124900179549001796AG29GENIChomozygous50230664
124900180749001808CT30GENIChomozygous50230666
124900218949002190TC31GENIChomozygous50230668
124900231749002318CT22GENIChomozygous50230670
124900276149002765TCTG----32GENIChomozygous50230672
124900290849002909TC43GENIChomozygous50230674
124900297849002979TC36GENIChomozygous50230676
124900320149003202TC17GENIChomozygous50230678
124900352449003525C-10GENIChomozygous50230682
124900377849003779CT23GENIChomozygous50230685
124900380749003809TC--18GENICheterozygous50546588
124900411949004126AAAAAAA-------9GENICheterozygous50230687
124900425049004251TG23GENIChomozygous50230689
124900425149004252CT23GENIChomozygous50230691
124900430549004306TA23GENIChomozygous50230693
124900438149004382CG21GENIChomozygous50230695
124900486249004863TTA9GENIChomozygous50230697
124899078848990789AATCAGTTGGGCGTGCTGATGGGCACGTACCTCTTCCAACG45GENIChomozygous50513686
124900411849004126AAAAAAAA--------9GENICpossibly homozygous50343634