chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2226581748226581749CT13GENIChomozygous74422188
2226581770226581771CA13GENIChomozygous74422191
2226581787226581788CG18GENIChomozygous74422194
2226581831226581832AG16GENIChomozygous74422197
2226581980226581981GA17GENIChomozygous75716548
2226582886226582887AG14GENIChomozygous74422200
2226583585226583586GC11GENIChomozygous74422203
2226586308226586309CT16GENIChomozygous74422212
2226587018226587019GA10GENIChomozygous74422218
2226587203226587204CA12GENIChomozygous75716550
2226588189226588190CT8GENIChomozygous75716556
2226588526226588527CT8GENIChomozygous74422227
2226589566226589567AC12GENIChomozygous75716558
2226590916226590917TG3GENIChomozygous74422233
2226593899226593900GT19GENIChomozygous74422251
2226596535226596536TA6GENIChomozygous75716569
2226597654226597655AG4GENIChomozygous74422266
2226597738226597739GA13GENICpossibly homozygous74422269
2226597792226597793GA8GENICpossibly homozygous75716571
2226598656226598657GT17GENIChomozygous74933586
2226598781226598782AT5GENIChomozygous74933587
2226599262226599263CT8GENIChomozygous74933588
2226599804226599805CG3GENIChomozygous75716573
2226599879226599880GA4GENIChomozygous74933590
2226599889226599890TC7GENIChomozygous74933591