chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71217539212175398GACCCG------26GENIChomozygous53790331
71217600412176005CT41GENIChomozygous53790332
71217613312176134AC33GENIChomozygous53790333
71217683512176836A-27GENIChomozygous53790334
71217847512178476AC25GENIChomozygous53790335
71217891612178917TTGTGC17GENIChomozygous53790336
71217930112179302TTG11GENICpossibly homozygous53790337
71218015312180171GCAGCGGTCGCCTCCACT------------------31GENIChomozygous53790338
71218046912180470GA27GENIChomozygous53790339
71218051312180514CT28GENIChomozygous53790340
71218056812180569CT23GENIChomozygous53790341
71218079112180792GA17GENIChomozygous53790342
71218128412181285CT34GENIChomozygous53790343
71218365512183656TTC18GENIChomozygous53790344