chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4140887210140887211TG11GENIChomozygous112858184
4140887405140887406GC36GENIChomozygous112858186
4140887526140887527AG36GENIChomozygous112858188
4140888936140888937TC2GENIChomozygous119465394
4140894149140894150GA40GENIChomozygous112858194
4140896988140896989GA36GENIChomozygous112858196
4140902715140902716TC26GENIChomozygous112858204
4140902957140902958AG14GENIChomozygous112858206
4140903807140903808CT19GENIChomozygous112858210
4140894483140894484TC30GENIChomozygous113057521
4140894658140894659GC33GENIChomozygous113057523
4140899328140899329GA27GENIChomozygous113057525
4140906395140906396AG31GENIChomozygous112858212
4140908274140908275TG22GENIChomozygous112858214
4140908994140908995GC35GENIChomozygous113057535
4140909042140909043GA24GENIChomozygous112858216
4140909059140909060CA32GENIChomozygous113057537
4140909109140909110GA30GENIChomozygous113057539
4140909129140909130CT30GENIChomozygous113057541
4140909170140909171GA24GENIChomozygous113057543
4140909196140909197CT28GENIChomozygous112858220
4140909244140909245GT40GENIChomozygous112858222
4140909248140909249TA41GENIChomozygous112858224
4140909269140909270GA40GENICpossibly homozygous113057545
4140909286140909287GC38GENIChomozygous113057547
4140913522140913523CT16GENIChomozygous113057549
4140916630140916631TG16GENIChomozygous112858250
4140916631140916632CA17GENIChomozygous112858252
4140916937140916938GA21GENIChomozygous113057551