chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1142721494142721495AG68GENIChomozygous108263822
1142721684142721685GA48GENICpossibly homozygous108263824
1142722114142722115TC66GENIChomozygous108263826
1142722292142722293TC49GENIChomozygous108263828
1142722297142722298TG48GENIChomozygous108263830
1142722420142722421CT60GENIChomozygous108263832
1142723117142723118CG52GENIChomozygous108263834
1142723956142723957GA49GENIChomozygous108263836
1142724171142724172CT58GENIChomozygous108263838