chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4140887210140887211TG23GENIChomozygous987832792
4140887405140887406GC28GENIChomozygous987832793
4140887526140887527AG34GENIChomozygous987832794
4140892114140892115TA24GENIChomozygous987832795
4140894149140894150GA20GENIChomozygous987832796
4140894483140894484TC27GENIChomozygous987832797
4140894658140894659GC39GENIChomozygous987832798
4140896988140896989GA24GENIChomozygous987832799
4140899328140899329GA26GENIChomozygous987832800
4140902715140902716TC28GENIChomozygous987832801
4140902957140902958AG29GENIChomozygous987832802
4140903807140903808CT10GENIChomozygous987832803
4140906395140906396AG41GENIChomozygous987832804
4140908274140908275TG24GENIChomozygous987832805
4140908994140908995GC15GENIChomozygous987832806
4140909042140909043GA21GENIChomozygous987832807
4140909059140909060CA26GENIChomozygous987832808
4140909109140909110GA31GENIChomozygous987832809
4140909196140909197CT34GENIChomozygous987832810
4140909244140909245GT30GENIChomozygous987832811
4140909248140909249TA29GENIChomozygous987832812
4140909269140909270GA31GENIChomozygous987832813
4140909286140909287GC31GENIChomozygous987832814
4140913522140913523CT21GENIChomozygous987832815
4140916630140916631TG17GENIChomozygous987832816
4140916631140916632CA17GENIChomozygous987832817
4140916937140916938GA29GENIChomozygous987832818