chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2226583585226583586GC8GENIChomozygous74422203
2226586308226586309CT24GENIChomozygous74422212
2226587031226587032CG29GENIChomozygous74422221
2226588526226588527CT32GENIChomozygous74422227
2226585975226585976CA47GENIChomozygous74933582
2226587829226587830AT12GENIChomozygous74933584
2226590328226590329CA15GENICpossibly homozygous74422230
2226590916226590917TG22GENIChomozygous74422233
2226591405226591406TC14GENIChomozygous74422239
2226592514226592515GA17GENIChomozygous74422245
2226593025226593026AT11GENICheterozygous74933585
2226593899226593900GT18GENIChomozygous74422251
2226593925226593926CG13GENIChomozygous74422254
2226594325226594326CA10GENIChomozygous74422257
2226596285226596286AG33GENIChomozygous74422263
2226597654226597655AG40GENIChomozygous74422266
2226597738226597739GA29GENIChomozygous74422269
2226598656226598657GT34GENIChomozygous74933586
2226598781226598782AT26GENIChomozygous74933587
2226599262226599263CT22GENIChomozygous74933588
2226599879226599880GA27GENIChomozygous74933590
2226599889226599890TC25GENIChomozygous74933591