chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1266866964266866965TG30GENIChomozygous960078781
1266867306266867307GA38GENIChomozygous960078782
1266869171266869172TC24GENIChomozygous960078783
1266869354266869355CT24GENIChomozygous960078784
1266871195266871196CT32GENIChomozygous960078785
1266871799266871800AG36GENIChomozygous960078786
1266872295266872296GA32GENIChomozygous960078787
1266876378266876379AG23GENIChomozygous960078788
1266876812266876813GA26GENIChomozygous960078789
1266878355266878356CT32GENIChomozygous960078790
1266879795266879796TG25GENIChomozygous960078791
1266879804266879805AG26GENIChomozygous960078792
1266881234266881235CT35GENIChomozygous960078793
1266881721266881722AG35GENIChomozygous960078794
1266882385266882386GC30GENIChomozygous960078795
1266884148266884149CG30GENIChomozygous960078796
1266885292266885293AC31GENIChomozygous960078797
1266885604266885605GA26GENIChomozygous960078798
1266887077266887078GA11GENIChomozygous960078799
1266888529266888530CT15GENIChomozygous960078800
1266889651266889652TC24GENIChomozygous960078801
1266890046266890047TC32GENIChomozygous960078802
1266892512266892513TC20GENIChomozygous960078803
1266894775266894776GA22GENIChomozygous960078804
1266895476266895477AG23GENIChomozygous960078805
1266896747266896748TG23GENIChomozygous960078806
1266897388266897389TC27GENIChomozygous960078807
1266897506266897507GA19GENIChomozygous960078808
1266898357266898358AG20GENIChomozygous960078809
1266899513266899514GA18GENIChomozygous960078810
1266907705266907706AT28GENIChomozygous960078811