chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124679952646799527TC48GENIChomozygous115342551
124680140446801405GC56GENIChomozygous115452027
124680141646801417GC58GENIChomozygous115396992
124680266146802662AG26GENIChomozygous115342553
124680344846803449GA58GENIChomozygous115342555
124680741746807418CT50GENIChomozygous115342557
124682787846827879TG22GENIChomozygous115342559
124683125046831251TC36GENIChomozygous115397078
124683138746831388CT45GENIChomozygous115342561
124683139046831391CG44GENIChomozygous115342563
124683414446834145TC34GENIChomozygous115452031
124684288446842885AG44GENIChomozygous115342565
124684486046844861GT27GENICpossibly homozygous115342567
124681187746811878TC52GENIChomozygous115444205
124683297246832973TG34GENICpossibly homozygous115444206
124682504246825043CT47GENICheterozygous118272499
124682835246828353CT33GENICheterozygous118272500
124682835446828355TC33GENICheterozygous118272501
124683111946831120AG19GENICheterozygous118272502
124683112546831126AG24GENICheterozygous118272503