chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2211004560211004561CG18GENIChomozygous110223871
2211006436211006437GC12GENIChomozygous111421046
2211008043211008044GA13GENIChomozygous110223875
2211008162211008163TC17GENIChomozygous110223876
2211008660211008661CT20GENIChomozygous110909039
2211009081211009082CT9GENIChomozygous110909040
2211009255211009256AG29GENIChomozygous110223877
2211010651211010652AT10GENICheterozygous110223880
2211010782211010783GC15GENIChomozygous110223881
2211010950211010951TC23GENIChomozygous110223882
2211011092211011093TC19GENIChomozygous110223883
2211011345211011346TC30GENIChomozygous110223884
2211011534211011535AC17GENIChomozygous110223885
2211011901211011902CT16GENIChomozygous110223886
2211012861211012862TC21GENIChomozygous110223887
2211013033211013034GA23GENIChomozygous110909042
2211013279211013280CT16GENIChomozygous111421047
2211013331211013332AG17GENIChomozygous110223888
2211013899211013900TC23GENIChomozygous110223890
2211013990211013991CT15GENIChomozygous110223891
2211014135211014136GA16GENIChomozygous110223892
2211014257211014258GA16GENIChomozygous111421048
2211014460211014461GA19GENIChomozygous110223893
2211015154211015155CT20GENIChomozygous110223894
2211015585211015586TC26GENIChomozygous110223896
2211016780211016781TC8GENIChomozygous110223897
2211016867211016868GA17GENIChomozygous110909044