chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2226581563226581564CG53GENICpossibly homozygous74422182
2226581641226581642GC48GENICpossibly homozygous74422185
2226581748226581749CT43GENIChomozygous74422188
2226581770226581771CA51GENIChomozygous74422191
2226581787226581788CG52GENICpossibly homozygous74422194
2226581831226581832AG52GENIChomozygous74422197
2226582886226582887AG40GENIChomozygous74422200
2226583585226583586GC36GENIChomozygous74422203
2226585310226585311TA39GENIChomozygous74422206
2226585785226585786CG15GENICheterozygous74422209
2226586308226586309CT43GENIChomozygous74422212
2226586992226586993GT39GENIChomozygous74422215
2226587018226587019GA40GENIChomozygous74422218
2226587031226587032CG41GENIChomozygous74422221
2226587668226587669TA24GENIChomozygous74422224
2226588526226588527CT65GENIChomozygous74422227
2226590328226590329CA35GENICheterozygous74422230
2226590916226590917TG50GENICpossibly homozygous74422233
2226591016226591017TC29GENIChomozygous74422236
2226591405226591406TC48GENIChomozygous74422239
2226591438226591439GT55GENICpossibly homozygous74422242
2226592514226592515GA62GENIChomozygous74422245
2226593459226593460AG36GENIChomozygous74422248
2226593899226593900GT68GENICpossibly homozygous74422251
2226593925226593926CG67GENIChomozygous74422254
2226594325226594326CA43GENIChomozygous74422257
2226596094226596095CT27GENIChomozygous74422260
2226596285226596286AG18GENIChomozygous74422263
2226597654226597655AG32GENIChomozygous74422266
2226597738226597739GA32GENICpossibly homozygous74422269