chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
MT1432414325TC2677GENICpossibly homozygous109049497
MT1448914490TC2761GENIChomozygous109024993
MT1458814589TA2749GENICpossibly homozygous109024996
MT1500515006AG2644GENIChomozygous109049499
MT1506215063TC2638GENIChomozygous109049502
MT1513515136AG2675GENIChomozygous109049505
MT1518815189CT2766GENIChomozygous109049507
MT1520915210CT2760GENIChomozygous109024998