chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
MT1060910610AG535GENIChomozygous109049485
MT1069610697CT422GENIChomozygous109024949
MT1112811129CA481GENICpossibly homozygous109024955
MT1137411375CA173GENIChomozygous129836993
MT1138911390AG163GENIChomozygous129836994