chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5177115066177115067CT43GENICpossibly homozygous55850320
5177115134177115135TA52GENICpossibly homozygous55850321
5177115261177115262TC43GENICpossibly homozygous55850322
5177115367177115368CT41GENICpossibly homozygous55850323
5177117876177117877GC41GENICpossibly homozygous55850324
5177118084177118085GA56GENIChomozygous55850325