chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10101291130101291131GA22GENIChomozygous51581698
10101291419101291420AG10GENIChomozygous51581700
10101291718101291719GA22GENIChomozygous51581702
10101291748101291749CT19GENIChomozygous51581704
10101291852101291853TC20GENIChomozygous51581706
10101291878101291879CG14GENIChomozygous51581708
10101293047101293048TC14GENIChomozygous51581710
10101293098101293100AC--3GENICheterozygous52446973
10101293269101293270T-20GENICpossibly homozygous51581712
10101293668101293676GTGTGTGT--------12GENIChomozygous51581714
10101293898101293899CT21GENIChomozygous51581716