chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
123224622932246230AACGCGCGCGCGCGCGCGCG12GENICpossibly homozygous50899392
123224630832246309GA35GENIChomozygous50442776
123224640632246428TGTGTGTGTGTGTGTGTGTGTG----------------------18GENIChomozygous50899393
123224644632246447TC10GENIChomozygous50442780
123224645532246456CCT13GENIChomozygous50442782
123224647032246471GA20GENIChomozygous50442784
123224667732246678AT31GENIChomozygous50442786
123224700132247002T-22GENIChomozygous50442788
123224700232247003TA22GENIChomozygous50672154
123224746532247466TC55GENIChomozygous50442790
123224760032247606TTATAT------5GENIChomozygous50899394
123224760632247607AG2GENIChomozygous50899395
123224813832248139TC4GENIChomozygous50442796
123224814132248142GA4GENIChomozygous50442798
123224815032248151GT5GENIChomozygous50442800
123224815532248156TA7GENIChomozygous50442802
123224815732248158GA8GENIChomozygous50442804
123224822832248229AT20GENIChomozygous50672156
123224830832248309AG18GENIChomozygous50442808
123224833132248332TG17GENIChomozygous50442810
123224839332248394GA19GENIChomozygous50442812
123224853732248538CT28GENIChomozygous50442814