chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2226581563226581564CG11GENIChomozygous74422182
2226581641226581642GC16GENIChomozygous74422185
2226581748226581749CT15GENIChomozygous74422188
2226581787226581788CG10GENIChomozygous74422194
2226582886226582887AG19GENIChomozygous74422200
2226583585226583586GC9GENIChomozygous74422203
2226584556226584557C6GENIChomozygous75855268
2226585310226585311TA6GENIChomozygous74422206
2226586308226586309CT20GENICpossibly homozygous74422212
2226586992226586993GT5GENIChomozygous74422215
2226587668226587669TA10GENIChomozygous74422224
2226587713226587714CA5GENIChomozygous75716554
2226588526226588527CT16GENIChomozygous74422227
2226590328226590329CA14GENIChomozygous74422230
2226590916226590917TG8GENIChomozygous74422233
2226591405226591406TC16GENIChomozygous74422239
2226591438226591439GT13GENIChomozygous74422242
2226592514226592515GA11GENIChomozygous74422245
2226593459226593460AG16GENIChomozygous74422248
2226593899226593900GT20GENIChomozygous74422251
2226593925226593926CG25GENIChomozygous74422254
2226594325226594326CA4GENIChomozygous74422257
2226595251226595252CG4GENIChomozygous75716563
2226597654226597655AG6GENIChomozygous74422266
2226589149226589149G14GENIChomozygous76003257