chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1264094064264094065AG17GENIChomozygous109217850
1264094170264094171GT24GENIChomozygous109217852
1264094261264094262TC37GENIChomozygous109217854
1264094954264094955GA26GENIChomozygous109217856
1264095002264095003TC16GENIChomozygous109217858
1264095870264095871CT20GENIChomozygous109217860
1264095886264095887AG23GENIChomozygous108783033
1264096067264096068CG25GENIChomozygous109217862
1264096228264096229CA21GENIChomozygous120782208
1264096229264096230AT22GENIChomozygous120782209
1264096802264096803GA29GENIChomozygous109217864
1264096893264096894CA19GENIChomozygous109217866
1264097432264097433TC8GENIChomozygous108783034
1264097484264097485TC17GENIChomozygous109217870
1264097567264097568GA24GENIChomozygous109217872
1264097573264097574GC24GENIChomozygous109217874
1264097633264097634AC24GENIChomozygous108635089
1264097768264097769AG30GENIChomozygous109217876
1264097829264097830TC33GENIChomozygous109217878
1264097921264097922AC21GENIChomozygous109217880
1264097923264097924AT21GENIChomozygous109217882
1264098124264098125TC20GENIChomozygous109217884
1264098178264098179GA28GENIChomozygous109217886
1264098215264098216TC21GENIChomozygous109217888
1264099322264099323TC12GENIChomozygous109217892
1264099341264099342AG12GENIChomozygous109217894
1264099343264099344AC12GENIChomozygous109217896
1264099366264099367GA13GENIChomozygous109217898
1264099541264099542GA24GENIChomozygous109217900
1264100050264100051GC20GENIChomozygous109217902
1264100146264100147TC3GENIChomozygous109217904
1264100637264100638TC20GENIChomozygous108783043
1264100900264100901TG23GENIChomozygous109217906
1264103344264103345CT20GENIChomozygous109217908