chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1266866964266866965TG28GENIChomozygous951545574
1266867306266867307GA39GENIChomozygous951545575
1266869171266869172TC24GENIChomozygous951545576
1266869354266869355CT29GENIChomozygous951545577
1266871195266871196CT19GENIChomozygous951545578
1266871799266871800AG37GENIChomozygous951545579
1266872295266872296GA22GENIChomozygous951545580
1266876378266876379AG28GENIChomozygous951545581
1266876812266876813GA24GENICpossibly homozygous951545582
1266878355266878356CT23GENIChomozygous951545583
1266879795266879796TG20GENIChomozygous951545584
1266881234266881235CT28GENIChomozygous951545585
1266881721266881722AG21GENIChomozygous951545586
1266882385266882386GC22GENIChomozygous951545587
1266884148266884149CG15GENIChomozygous951545588
1266885292266885293AC23GENIChomozygous951545589
1266885604266885605GA18GENIChomozygous951545590
1266885897266885898TC14GENIChomozygous951545591
1266887077266887078GA17GENIChomozygous951545592
1266888529266888530CT14GENIChomozygous951545593
1266889651266889652TC17GENIChomozygous951545594
1266890046266890047TC32GENIChomozygous951545595
1266892512266892513TC22GENIChomozygous951545596
1266894775266894776GA28GENIChomozygous951545597
1266895476266895477AG19GENIChomozygous951545598
1266896747266896748TG22GENICpossibly homozygous951545599
1266897388266897389TC25GENIChomozygous951545600
1266897506266897507GA19GENIChomozygous951545601
1266898357266898358AG30GENIChomozygous951545602
1266898962266898963GA6GENIChomozygous951545603
1266899513266899514GA21GENIChomozygous951545604
1266907705266907706AT30GENIChomozygous951545605