chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1264094064264094065AG30GENIChomozygous971745636
1264094170264094171GT33GENIChomozygous971745637
1264094261264094262TC13GENIChomozygous971745638
1264094954264094955GA21GENIChomozygous971745639
1264095002264095003TC18GENIChomozygous971745640
1264095870264095871CT23GENIChomozygous971745641
1264095886264095887AG24GENIChomozygous971745642
1264096067264096068CG26GENIChomozygous971745643
1264096228264096229CA24GENIChomozygous971745644
1264096229264096230AT23GENIChomozygous971745645
1264096802264096803GA34GENIChomozygous971745646
1264096893264096894CA16GENIChomozygous971745647
1264096989264096990AG12GENIChomozygous971745648
1264097432264097433TC33GENIChomozygous971745649
1264097484264097485TC26GENIChomozygous971745650
1264097567264097568GA15GENIChomozygous971745651
1264097573264097574GC14GENIChomozygous971745652
1264097633264097634AC12GENIChomozygous971745653
1264097768264097769AG18GENIChomozygous971745654
1264097829264097830TC15GENIChomozygous971745655
1264097921264097922AC15GENIChomozygous971745656
1264097923264097924AT14GENIChomozygous971745657
1264098124264098125TC23GENIChomozygous971745658
1264098178264098179GA16GENIChomozygous971745659
1264098215264098216TC13GENIChomozygous971745660
1264099322264099323TC23GENIChomozygous971745661
1264099341264099342AG27GENIChomozygous971745662
1264099343264099344AC26GENIChomozygous971745663
1264099366264099367GA27GENIChomozygous971745664
1264099541264099542GA15GENIChomozygous971745665
1264100050264100051GC14GENIChomozygous971745666
1264100637264100638TC11GENIChomozygous971745667
1264100900264100901TG10GENIChomozygous971745668
1264103344264103345CT18GENIChomozygous971745669