chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104740024447400245TC72GENIChomozygous116773595
104740118147401182TC39GENIChomozygous116773597
104740138747401388GC23GENIChomozygous117008804
104740266847402669TG54GENIChomozygous116773599
104740287447402875TC58GENIChomozygous116773601
104740141547401416AG23GENIChomozygous118036496
104740147047401473TGG44GENIChomozygous133228307
104740463747404641CTAT54GENICpossibly homozygous133228308
104740494347404944AG51GENIChomozygous116773603
104740681447406815TC48GENIChomozygous116773607
104740800047408001A43GENIChomozygous133228309
104740880647408807AG43GENIChomozygous116773609
104740896347408963AGGC29GENIChomozygous132691672
104740908947409090AG53GENIChomozygous116773611
104740913647409137GA60GENIChomozygous116773613
104740925347409253T70GENICpossibly homozygous132691673
104740961547409616AG56GENIChomozygous116773615
104740967547409676GC48GENIChomozygous116773617
104741535447415355G10GENIChomozygous133228310
104741907147419072GA60GENIChomozygous116773635
104741423947414240AG54GENIChomozygous116773619
104741581047415811AG50GENIChomozygous116773621
104741618547416186GA47GENIChomozygous116773623
104741637547416376AG59GENIChomozygous116773625
104741710347417104TC60GENIChomozygous116773627
104741808147418082AG55GENIChomozygous116773629
104741827347418274CT55GENIChomozygous116773631
104740359047403591TC23GENICheterozygous117218325
104740359147403592GA23GENICheterozygous131905502
104741928247419283AG37GENIChomozygous116773637
104741935047419351CT52GENIChomozygous116878587
104742092147420922GA47GENIChomozygous117008805
104742276347422764TC51GENIChomozygous116878589