chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10101291130101291131GA19GENIChomozygous51581698
10101291419101291420AG9GENICpossibly homozygous51581700
10101291718101291719GA11GENICpossibly homozygous51581702
10101291748101291749CT16GENICpossibly homozygous51581704
10101291852101291853TC13GENIChomozygous51581706
10101291878101291879CG11GENICpossibly homozygous51581708
10101293047101293048TC14GENICpossibly homozygous51581710
10101293269101293270T-8GENIChomozygous51581712
10101293898101293899CT13GENIChomozygous51581716