chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1264094064264094065AG58GENIChomozygous109217850
1264094170264094171GT40GENIChomozygous109217852
1264094261264094262TC28GENIChomozygous109217854
1264094954264094955GA22GENIChomozygous109217856
1264095002264095003TC24GENIChomozygous109217858
1264095870264095871CT30GENIChomozygous109217860
1264095886264095887AG30GENIChomozygous108783033
1264096067264096068CG20GENIChomozygous109217862
1264096228264096229CA35GENIChomozygous120782208
1264096229264096230AT35GENIChomozygous120782209
1264096802264096803GA31GENIChomozygous109217864
1264096893264096894CA42GENIChomozygous109217866
1264096989264096990AG29GENICpossibly homozygous109217868
1264097432264097433TC55GENIChomozygous108783034
1264097484264097485TC60GENIChomozygous109217870
1264097567264097568GA44GENIChomozygous109217872
1264097573264097574GC45GENIChomozygous109217874
1264097633264097634AC58GENIChomozygous108635089
1264097768264097769AG48GENIChomozygous109217876
1264097829264097830TC44GENIChomozygous109217878
1264097921264097922AC57GENIChomozygous109217880
1264097923264097924AT57GENIChomozygous109217882
1264098124264098125TC47GENIChomozygous109217884
1264098178264098179GA61GENIChomozygous109217886
1264098215264098216TC47GENIChomozygous109217888
1264099322264099323TC19GENIChomozygous109217892
1264099341264099342AG19GENIChomozygous109217894
1264099343264099344AC18GENIChomozygous109217896
1264099366264099367GA17GENIChomozygous109217898
1264099541264099542GA27GENIChomozygous109217900
1264100050264100051GC23GENIChomozygous109217902
1264100637264100638TC43GENIChomozygous108783043
1264100900264100901TG32GENIChomozygous109217906
1264103344264103345CT32GENIChomozygous109217908