chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
MT72067207TC2609GENIChomozygous109058800
MT72277228TC2670GENICpossibly homozygous120180390
MT72997300GA2750GENIChomozygous109024926
MT74017402AG2862GENICpossibly homozygous109058801
MT74557456CT2756GENICpossibly homozygous109049459
MT75787579AG2712GENIChomozygous109058802
MT76477648CG2627GENIChomozygous109024929