chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2226581563226581564CG41GENIChomozygous74422182
2226581641226581642GC44GENIChomozygous74422185
2226581748226581749CT50GENIChomozygous74422188
2226581770226581771CA44GENIChomozygous74422191
2226581787226581788CG46GENIChomozygous74422194
2226581831226581832AG47GENIChomozygous74422197
2226582886226582887AG50GENIChomozygous74422200
2226583585226583586GC13GENIChomozygous74422203
2226585310226585311TA41GENIChomozygous74422206
2226586308226586309CT47GENIChomozygous74422212
2226586992226586993GT27GENIChomozygous74422215
2226587018226587019GA28GENIChomozygous74422218
2226587031226587032CG31GENIChomozygous74422221
2226588526226588527CT36GENIChomozygous74422227
2226590328226590329CA32GENICheterozygous74422230
2226590916226590917TG41GENIChomozygous74422233
2226591405226591406TC38GENIChomozygous74422239
2226591438226591439GT37GENIChomozygous74422242
2226592514226592515GA29GENIChomozygous74422245
2226593459226593460AG37GENIChomozygous74422248
2226593899226593900GT32GENIChomozygous74422251
2226593925226593926CG34GENIChomozygous74422254
2226594325226594326CA29GENICpossibly homozygous74422257
2226596094226596095CT21GENIChomozygous74422260
2226596285226596286AG17GENIChomozygous74422263
2226597654226597655AG33GENIChomozygous74422266
2226597738226597739GA42GENIChomozygous74422269