chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
MT1382213823CT2536GENICpossibly homozygous109049494
MT1385813859CT2479GENICpossibly homozygous120177779
MT1387913880CA2477GENICpossibly homozygous109024987
MT1397413975GA2701GENICpossibly homozygous109024989