chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10101288987101288997TGTATGTATG----------7GENICheterozygous51581694
10101288988101288994GTATGT------7GENICheterozygous51760376
10101288991101288997TGTATG------9GENICpossibly homozygous51581696
10101291130101291131GA54GENIChomozygous51581698
10101291419101291420AG18GENICpossibly homozygous51581700
10101291718101291719GA26GENIChomozygous51581702
10101291748101291749CT30GENIChomozygous51581704
10101291852101291853TC40GENIChomozygous51581706
10101291878101291879CG38GENIChomozygous51581708
10101293047101293048TC37GENIChomozygous51581710
10101293269101293270T-24GENIChomozygous51581712
10101293668101293676GTGTGTGT--------3GENIChomozygous51581714
10101293898101293899CT39GENIChomozygous51581716