chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2189088661189088662CG17GENIChomozygous110804852
2189089286189089287CT9GENIChomozygous110804853
2189089408189089409TC14GENIChomozygous110804854
2189089857189089858AG15GENIChomozygous110804855
2189090629189090630GA21GENIChomozygous110804856
2189090790189090791CT20GENIChomozygous110804857
2189091069189091070GA12GENIChomozygous110804858
2189091371189091372GA9GENIChomozygous110804859
2189091509189091510GA9GENIChomozygous110906288
2189091689189091690AG18GENIChomozygous110804860
2189092691189092692GA14GENICpossibly homozygous110804861
2189092780189092781CT22GENICpossibly homozygous110804862
2189094018189094019TC19GENIChomozygous110804863
2189095722189095723CT9GENIChomozygous110170814
2189094905189094906TA23GENIChomozygous110170811
2189095347189095348CT20GENIChomozygous110170812