chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71217539212175398GACCCG------21GENIChomozygous53790331
71217613312176134AC51GENIChomozygous53790333
71217636212176363GA51GENIChomozygous54629991
71217847512178476AC47GENIChomozygous53790335
71217891612178917TTGTGC26GENIChomozygous53790336
71217930112179302TTG29GENICpossibly homozygous53790337
71218015312180171GCAGCGGTCGCCTCCACT------------------61GENIChomozygous53790338
71218046912180470GA26GENIChomozygous53790339
71218051312180514CT32GENIChomozygous53790340
71218056812180569CT38GENIChomozygous53790341
71218079112180792GA64GENIChomozygous53790342
71218128412181285CT50GENIChomozygous53790343
71218365512183656TTC27GENIChomozygous53790344