chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71217539212175398GACCCG------1GENIChomozygous53790331
71217600412176005CT12GENICpossibly homozygous53790332
71217613312176134AC22GENIChomozygous53790333
71217683512176836A-17GENIChomozygous53790334
71217891612178917TTGTGC7GENICpossibly homozygous53790336
71217930112179302TTG2GENIChomozygous53790337
71218015312180171GCAGCGGTCGCCTCCACT------------------1GENIChomozygous53790338
71218046912180470GA18GENIChomozygous53790339
71218051312180514CT11GENIChomozygous53790340
71218056812180569CT12GENICheterozygous53790341
71218079112180792GA17GENIChomozygous53790342
71218128412181285CT7GENICheterozygous53790343
71218365512183656TTC8GENICheterozygous53790344