chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
15307137953071380GT21GENIChomozygous108850471
15307211853072119TC25GENIChomozygous108850475
15307290653072907GA23GENIChomozygous108850478
15307376753073768CT14GENIChomozygous109077775
15307389153073892GA16GENIChomozygous108850485
15307417153074172GA30GENIChomozygous109077777
15307564053075641GT28GENIChomozygous109077779
15307567653075677TC27GENIChomozygous108850495
15307643553076436CT24GENIChomozygous109077781
15307649853076499CT32GENIChomozygous108850502
15307700653077007CT26GENIChomozygous109077783
15307717553077176CT31GENIChomozygous109077785
15307742853077429TC44GENIChomozygous109077787
15307799553077996TA26GENIChomozygous109077789
15307934453079345CT31GENIChomozygous109077791
15308065953080660CT23GENIChomozygous108850514
15308125553081256TC27GENIChomozygous108850516
15308163353081634GA21GENIChomozygous108850519
15308258253082583CT33GENIChomozygous109077793
15308264353082644TA23GENIChomozygous108850524
15308355453083555CT21GENIChomozygous109077795
15308384053083841GA25GENIChomozygous109077797
15308398053083981GT24GENIChomozygous109077799
15308429253084293TC23GENIChomozygous109077801
15308434153084342TG24GENIChomozygous109077803
15308435053084351TG21GENIChomozygous109077805
15308510453085105GA36GENIChomozygous109077807
15308517253085173GA31GENIChomozygous108850535
15308545853085459GA26GENIChomozygous109077809
15308570253085703AG19GENIChomozygous109077811
15308629753086298GC25GENIChomozygous109077813
15308699453086995AG33GENIChomozygous109077825
15308724053087241AG31GENIChomozygous108850542
15308731353087314AG25GENICpossibly homozygous109077827
15308750953087510GA37GENIChomozygous109077829