chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1207906927207906928TC17GENIChomozygous184598916
1207908248207908249GA17GENIChomozygous184598917
1207908630207908631AG20GENICpossibly homozygous184598918
1207908909207908910AG18GENICpossibly homozygous184598919
1207909303207909304GT18GENIChomozygous184598920
1207910695207910696CT4GENIChomozygous184598921
1207910812207910813AG4GENIChomozygous184598922
1207910871207910872GA7GENICheterozygous184598923
1207912138207912139AG15GENIChomozygous184598924
1207916744207916745CA15GENIChomozygous184598925
1207917431207917432AC6GENICheterozygous184598926
1207917463207917464GA12GENIChomozygous184598927
1207918103207918104AG10GENIChomozygous184598928
1207919523207919524GT17GENIChomozygous184598929
1207920773207920774GA21GENIChomozygous184598930
1207921899207921900TC13GENIChomozygous184598931
1207922094207922095AG8GENIChomozygous184598932
1207923799207923800GC22GENIChomozygous184598933
1207923809207923810GA21GENIChomozygous184598934
1207924348207924349TC10GENIChomozygous184598935