chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7117589987117589988TC15GENICpossibly homozygous54078154
7117590227117590228AG17GENICpossibly homozygous54078155
7117590918117590919AG10GENICheterozygous54078157
7117591549117591550TG21GENICpossibly homozygous54078158