chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10101288988101288990GT--7GENIChomozygous52446971
10101288991101288997TGTATG------8GENICpossibly homozygous51581696
10101291130101291131GA14GENIChomozygous51581698
10101291419101291420AG6GENIChomozygous51581700
10101291718101291719GA17GENIChomozygous51581702
10101291748101291749CT19GENIChomozygous51581704
10101291852101291853TC24GENIChomozygous51581706
10101291878101291879CG22GENIChomozygous51581708
10101293047101293048TC18GENIChomozygous51581710
10101293098101293100AC--2GENIChomozygous52446973
10101293269101293270T-27GENIChomozygous51581712
10101293668101293676GTGTGTGT--------8GENIChomozygous51581714
10101293898101293899CT29GENIChomozygous51581716