chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7117589987117589988TC13GENICpossibly homozygous54078154
7117590227117590228AG23GENICpossibly homozygous54078155
7117590918117590919AG10GENICpossibly homozygous54078157
7117591549117591550TG25GENICpossibly homozygous54078158
7117591884117591885CT6GENICheterozygous54078159