chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3147503976147503977AAT63GENIChomozygous57727510
3147506203147506206GAT---8GENIChomozygous57727512
3147506245147506246GA17GENIChomozygous57727514
3147506708147506709CCT41GENIChomozygous57727516
3147507467147507468CG46GENIChomozygous57727518
3147507762147507763T-30GENIChomozygous57727520
3147508105147508106GA55GENIChomozygous57727522
3147508526147508527GT28GENIChomozygous57727524
3147508614147508616TT--10GENIChomozygous57727526
3147514338147514339GT15GENICpossibly homozygous57727528
3147514505147514506CG51GENICheterozygous57727530
3147515147147515148TG44GENICpossibly homozygous57727532
3147515346147515347TC48GENIChomozygous57727534
3147515844147515846AA--12GENICheterozygous57727536
3147515918147515926TCTCTCTC--------24GENICheterozygous58039389
3147515952147515955TCT---30GENIChomozygous57727538
3147516163147516164AG33GENICpossibly homozygous57727540
3147517282147517283TG49GENICpossibly homozygous57727542
3147517341147517342AG44GENIChomozygous57727544
3147517344147517345GA44GENIChomozygous57727546
3147517411147517412CT39GENICpossibly homozygous57727548
3147517442147517443CT45GENIChomozygous57727550