chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1206729009206729010T-40GENIChomozygous62096273
1206729625206729626TC20GENIChomozygous61067683
1206729949206729950CCT24GENIChomozygous62695138
1206729972206729973AG22GENIChomozygous61067684
1206730000206730001GA20GENIChomozygous62096274
1206730001206730002CA20GENIChomozygous62096275
1206730442206730443AG12GENIChomozygous61067686
1206730589206730590AG15GENIChomozygous61067687
1206731111206731112GA26GENIChomozygous62096276
1206731246206731247CT24GENIChomozygous62096277
1206731429206731430GC26GENIChomozygous61067688
1206731862206731863AG17GENIChomozygous61067689
1206732495206732496AT25GENIChomozygous62096278
1206732496206732497CT23GENIChomozygous62096279
1206732769206732770AG20GENIChomozygous61067693
1206732894206732895CT18GENIChomozygous62096280
1206733076206733077GT19GENIChomozygous62096281
1206733334206733335AG15GENIChomozygous61067694
1206733970206733971TC14GENIChomozygous61067695
1206734024206734025TC16GENIChomozygous61067696