chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4100213330100213337GACTTCT48GENICpossibly homozygous131357422
4100213631100213632AG36GENIChomozygous112798368
4100214547100214548CT49GENIChomozygous112798370
4100215137100215138TC53GENIChomozygous112798372
4100215098100215099GA59GENIChomozygous119523781