chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10101288987101288997TGTATGTATG----------14GENICpossibly homozygous51581694
10101288991101288997TGTATG------14GENICpossibly homozygous51581696
10101291130101291131GA45GENIChomozygous51581698
10101291419101291420AG31GENICpossibly homozygous51581700
10101291718101291719GA55GENIChomozygous51581702
10101291748101291749CT44GENIChomozygous51581704
10101291852101291853TC52GENICpossibly homozygous51581706
10101291878101291879CG46GENIChomozygous51581708
10101293047101293048TC43GENIChomozygous51581710
10101293269101293270T-38GENIChomozygous51581712
10101293668101293676GTGTGTGT--------5GENIChomozygous51581714
10101293898101293899CT60GENIChomozygous51581716