chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
MT79307931CT984GENICpossibly homozygous109049470
MT80218022GA942GENICpossibly homozygous120180392
MT83268327CA1025GENIChomozygous109024934
MT83448345TC1033GENIChomozygous109024937
MT85458546TC1052GENIChomozygous133464007