chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1156200949156200950AG56GENIChomozygous135716288
1156201644156201645TC40GENIChomozygous135716289
1156202758156202759AT27GENIChomozygous135716290
1156203776156203777GA24GENIChomozygous141265617
1156204376156204377CT54GENIChomozygous135716292
1156204661156204662GA44GENIChomozygous135716293
1156205781156205782CT46GENIChomozygous141265618
1156206431156206432TG41GENICpossibly homozygous135716294
1156210741156210742AG58GENIChomozygous135716296
1156210753156210754GA52GENIChomozygous135716297
1156213435156213436A22GENIChomozygous140958709
1156214704156214705CG38GENIChomozygous135716299
1156216263156216264CT47GENIChomozygous135716300
1156216982156216983TC40GENIChomozygous135716301
1156202369156202370CT41GENIChomozygous143793286
1156205454156205455C15GENICheterozygous402969228
1156205454156205455CA15GENICheterozygous402969229