chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2211003489211003490CT23GENIChomozygous110223867
2211004174211004175CT22GENIChomozygous110223868
2211004475211004476CT26GENIChomozygous110223869
2211004559211004560AG26GENIChomozygous110223870
2211004560211004561CG27GENIChomozygous110223871
2211005392211005393GA34GENIChomozygous110223872
2211006487211006488GA18GENIChomozygous110223873
2211007247211007248GA26GENIChomozygous110621612
2211007805211007806CT27GENIChomozygous110223874
2211008043211008044GA31GENIChomozygous110223875
2211008162211008163TC20GENIChomozygous110223876
2211009255211009256AG16GENIChomozygous110223877
2211009911211009912TC2GENIChomozygous110223878
2211010010211010011AG12GENIChomozygous110223879
2211010651211010652AT26GENIChomozygous110223880
2211010782211010783GC31GENIChomozygous110223881
2211010950211010951TC23GENIChomozygous110223882
2211011092211011093TC26GENIChomozygous110223883
2211011345211011346TC28GENIChomozygous110223884
2211011534211011535AC42GENIChomozygous110223885
2211011901211011902CT21GENIChomozygous110223886
2211012861211012862TC19GENIChomozygous110223887
2211013331211013332AG22GENIChomozygous110223888
2211013855211013856AG31GENIChomozygous110223889
2211013899211013900TC29GENIChomozygous110223890
2211013990211013991CT34GENIChomozygous110223891
2211014135211014136GA17GENIChomozygous110223892
2211014460211014461GA14GENICpossibly homozygous110223893
2211015154211015155CT26GENIChomozygous110223894
2211015243211015244GA23GENIChomozygous110223895
2211015585211015586TC14GENIChomozygous110223896
2211016780211016781TC22GENIChomozygous110223897