chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1205930160205930161TTAGC25GENIChomozygous745952330
1205930416205930417CT34GENIChomozygous632079874
1205930522205930523CT22GENIChomozygous632079875
1205930588205930590TC--7GENIChomozygous745952331
1205930695205930696C-10GENIChomozygous745952332
1205931009205931010CT24GENIChomozygous632079876
1205931569205931570AG37GENICpossibly homozygous632079877
1205931907205931908GA47GENIChomozygous632079878
1205933575205933576TTG28GENIChomozygous745952333
1205934239205934240AC26GENICpossibly homozygous632079879
1205934704205934705AG31GENICpossibly homozygous632079880
1205936755205936756GA23GENIChomozygous632079881
1205937469205937470AG18GENIChomozygous632079882
1205938362205938364GT--25GENIChomozygous745952334