chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2226583585226583586GC13GENIChomozygous74422203
2226585975226585976CA44GENIChomozygous74933582
2226586308226586309CT20GENIChomozygous74422212
2226587031226587032CG35GENIChomozygous74422221
2226587829226587830AT35GENIChomozygous74933584
2226588526226588527CT44GENIChomozygous74422227
2226590328226590329CA20GENICpossibly homozygous74422230
2226590916226590917TG26GENIChomozygous74422233
2226591405226591406TC27GENIChomozygous74422239
2226592514226592515GA18GENIChomozygous74422245
2226593025226593026AT21GENIChomozygous74933585
2226593899226593900GT25GENIChomozygous74422251
2226593925226593926CG27GENIChomozygous74422254
2226594325226594326CA21GENIChomozygous74422257
2226596285226596286AG21GENIChomozygous74422263
2226597654226597655AG35GENIChomozygous74422266
2226597738226597739GA27GENIChomozygous74422269
2226598656226598657GT26GENIChomozygous74933586
2226598781226598782AT34GENIChomozygous74933587
2226599262226599263CT25GENIChomozygous74933588
2226599879226599880GA44GENIChomozygous74933590
2226599889226599890TC46GENIChomozygous74933591