chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1141460855141460856CT28GENIChomozygous108260709
1141461017141461018GA31GENICpossibly homozygous108260711
1141461408141461409CT13GENIChomozygous108260715
1141461836141461837AG22GENIChomozygous108260717
1141462004141462005TG8GENIChomozygous108260719
1141462062141462063CT8GENICheterozygous108260721
1141462063141462064GA8GENICheterozygous108260723
1141462304141462305GA21GENIChomozygous108260725
1141462562141462563CA22GENIChomozygous108260727
1141462563141462564TA22GENIChomozygous108260729
1141462772141462773CT15GENIChomozygous108260731
1141463107141463108CT15GENIChomozygous108260733
1141463155141463156TA15GENIChomozygous108260735
1141463741141463742CT55GENIChomozygous108260737
1141463846141463847AG36GENIChomozygous108260739
1141465077141465078GA51GENICheterozygous108260745
1141465096141465097AG46GENICpossibly homozygous108260747
1141466076141466077TC28GENIChomozygous108260749
1141466276141466277GA24GENIChomozygous108260751
1141466297141466298GA20GENIChomozygous108260753
1141466334141466335TC19GENIChomozygous108260755
1141468350141468351AG22GENIChomozygous108260757
1141470436141470437TC24GENIChomozygous108260759
1141470774141470775TC18GENIChomozygous108260761