chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4140887405140887406GC19GENIChomozygous934892658
4140887526140887527AG11GENIChomozygous934892659
4140892114140892115TA15GENIChomozygous934892660
4140894149140894150GA24GENIChomozygous934892661
4140894483140894484TC25GENIChomozygous934892662
4140894658140894659GC22GENIChomozygous934892663
4140896988140896989GA19GENIChomozygous934892664
4140899328140899329GA19GENIChomozygous934892665
4140902715140902716TC25GENIChomozygous934892666
4140902957140902958AG23GENIChomozygous934892667
4140903807140903808CT26GENIChomozygous934892668
4140906395140906396AG23GENIChomozygous934892669
4140908274140908275TG20GENIChomozygous934892670
4140908994140908995GC24GENIChomozygous934892671
4140909042140909043GA18GENICpossibly homozygous934892672
4140909059140909060CA23GENIChomozygous934892673
4140909109140909110GA34GENIChomozygous934892674
4140909129140909130CT35GENICpossibly homozygous934892675
4140909170140909171GA25GENIChomozygous934892676
4140909196140909197CT25GENIChomozygous934892677
4140909244140909245GT24GENIChomozygous934892678
4140909248140909249TA24GENIChomozygous934892679
4140909269140909270GA24GENIChomozygous934892680
4140913522140913523CT8GENIChomozygous934892681
4140916630140916631TG24GENIChomozygous934892682
4140916631140916632CA24GENIChomozygous934892683
4140916937140916938GA30GENIChomozygous934892684