chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
MT79307931CT3120GENICpossibly homozygous109049470
MT79817982AG3230GENICpossibly homozygous109049473
MT81558156TC3158GENICpossibly homozygous109024931
MT83268327CA3205GENICpossibly homozygous109024934
MT83448345TC3246GENIChomozygous109024937
MT84528453TC3252GENICpossibly homozygous109049476