chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3147503976147503977AAT58GENIChomozygous57727510
3147506203147506206GAT---22GENIChomozygous57727512
3147506245147506246GA50GENIChomozygous57727514
3147506708147506709CCT65GENIChomozygous57727516
3147507467147507468CG58GENIChomozygous57727518
3147507762147507763T-41GENICpossibly homozygous57727520
3147508105147508106GA105GENICpossibly homozygous57727522
3147508526147508527GT50GENIChomozygous57727524
3147508614147508616TT--12GENIChomozygous57727526
3147514338147514339GT21GENIChomozygous57727528
3147514505147514506CG62GENICheterozygous57727530
3147515147147515148TG66GENICpossibly homozygous57727532
3147515346147515347TC58GENIChomozygous57727534
3147515844147515846AA--30GENICheterozygous57727536
3147515918147515926TCTCTCTC--------24GENICheterozygous58039389
3147515952147515955TCT---29GENICpossibly homozygous57727538
3147516163147516164AG63GENIChomozygous57727540
3147517282147517283TG42GENIChomozygous57727542
3147517341147517342AG42GENIChomozygous57727544
3147517344147517345GA45GENIChomozygous57727546
3147517411147517412CT57GENIChomozygous57727548
3147517442147517443CT63GENIChomozygous57727550