chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5151776814151776816CC--7GENICpossibly homozygous55797521
5151776832151776833GA8GENICheterozygous55797522
5151776878151776879TC15GENICheterozygous55925739
5151777410151777411GA19GENIChomozygous55797523
5151777616151777617CCT10GENICpossibly homozygous55797524
5151777773151777777TGTG----7GENIChomozygous55797525