chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
28695978386959784TC56GENIChomozygous136204143
28696008286960083AG47GENICpossibly homozygous136204144
28696014086960141CA36GENICpossibly homozygous136204145
28696086386960864TC56GENICpossibly homozygous136204146
28696087386960874TC54GENICpossibly homozygous136204147
28696093386960934TC60GENIChomozygous136204148
28696104486961045AG50GENICpossibly homozygous136204149
28696109986961100GT49GENIChomozygous146043667
28696119986961200TA45GENICpossibly homozygous136204150
28696130686961307AG36GENIChomozygous136204151
28696157286961573GA53GENIChomozygous141396532
28696170786961708GC45GENIChomozygous136204153
28696171386961714AG45GENIChomozygous136204154
28696175786961758GC42GENIChomozygous146043668
28696205386962054GA44GENIChomozygous136204155
28696220486962205TC40GENIChomozygous136204156
28696220586962206GT40GENIChomozygous136204157
28696273186962732AC39GENICpossibly homozygous136204158
28696281486962815TC53GENIChomozygous146043669
28696136286961363GA36GENICheterozygous153962659
28696251986962520GT24GENIChomozygous153962660
28696136286961363G36GENICpossibly homozygous403556916
28696371686963717AT46GENIChomozygous136204160
28696379986963800CG43GENIChomozygous136204161
28696383986963840CT34GENIChomozygous146043670
28696389486963895TC34GENIChomozygous136204162
28696407986964080TC49GENIChomozygous136204163
28696426286964263AG40GENIChomozygous136204164
28696484386964844GT31GENIChomozygous136204165
28696511486965115TC62GENIChomozygous136204166
28696511586965116AG64GENIChomozygous136204167
28696530386965304TC44GENIChomozygous136204168
28696536686965367CT46GENIChomozygous136204169
28696606586966066TG61GENIChomozygous146043671
28696611086966111TC58GENIChomozygous136204170
28696674086966741TC45GENIChomozygous136204172
28696728086967281TA37GENIChomozygous136204173
28696728286967283TG38GENIChomozygous136204174