chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
979716757971676TC18GENICpossibly homozygous186981448
979761837976184AG16GENIChomozygous185215894
979792057979206GA17GENIChomozygous185215895
979799477979948CT24GENIChomozygous186981449
979844257984426TC18GENIChomozygous186981450
979844267984427TC18GENIChomozygous186981451
979892627989263CT16GENIChomozygous185215896
979933767993377GA3GENIChomozygous185215897
979934747993475AG18GENIChomozygous185215898