chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1206729009206729010T-26GENICpossibly homozygous62096273
1206729625206729626TC22GENIChomozygous61067683
1206729972206729973AG16GENICpossibly homozygous61067684
1206730000206730001GA22GENICpossibly homozygous62096274
1206730001206730002CA22GENICpossibly homozygous62096275
1206730442206730443AG30GENICpossibly homozygous61067686
1206730589206730590AG26GENICpossibly homozygous61067687
1206731111206731112GA22GENIChomozygous62096276
1206731246206731247CT20GENICpossibly homozygous62096277
1206731429206731430GC21GENIChomozygous61067688
1206731862206731863AG32GENIChomozygous61067689
1206732495206732496AT26GENIChomozygous62096278
1206732496206732497CT26GENIChomozygous62096279
1206732769206732770AG23GENICpossibly homozygous61067693
1206732894206732895CT31GENICpossibly homozygous62096280
1206733076206733077GT28GENICpossibly homozygous62096281
1206733334206733335AG18GENIChomozygous61067694
1206733970206733971TC29GENICpossibly homozygous61067695
1206734024206734025TC32GENICpossibly homozygous61067696
1206729949206729950CCT22GENICpossibly homozygous62695138