chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10101288987101288997TGTATGTATG----------13GENICheterozygous51581694
10101288988101288994GTATGT------13GENICheterozygous51760376
10101288991101288997TGTATG------12GENICheterozygous51581696
10101291130101291131GA18GENIChomozygous51581698
10101291419101291420AG19GENIChomozygous51581700
10101291718101291719GA27GENIChomozygous51581702
10101291748101291749CT22GENIChomozygous51581704
10101291852101291853TC23GENIChomozygous51581706
10101291878101291879CG24GENIChomozygous51581708
10101293047101293048TC17GENIChomozygous51581710
10101293269101293270T-16GENIChomozygous51581712
10101293668101293676GTGTGTGT--------3GENIChomozygous51581714
10101293898101293899CT15GENIChomozygous51581716