chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10101288987101288993TGTATG------9GENICheterozygous53077448
10101288988101288990GT--9GENICheterozygous52446971
10101288991101288997TGTATG------11GENICheterozygous51581696
10101291130101291131GA51GENIChomozygous51581698
10101291419101291420AG13GENIChomozygous51581700
10101291718101291719GA19GENIChomozygous51581702
10101291748101291749CT24GENIChomozygous51581704
10101291852101291853TC38GENIChomozygous51581706
10101291878101291879CG36GENIChomozygous51581708
10101293047101293048TC30GENIChomozygous51581710
10101293269101293270T-19GENICpossibly homozygous51581712
10101293668101293676GTGTGTGT--------17GENIChomozygous51581714
10101293898101293899CT39GENIChomozygous51581716