chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1263505776263505777GA45GENIChomozygous108633188
1263505878263505879GA51GENICpossibly homozygous108633190
1263505886263505887CT48GENIChomozygous108633192
1263505907263505908GA46GENIChomozygous108633194
1263505920263505921GA53GENICpossibly homozygous108633195
1263505944263505945GA43GENICpossibly homozygous108633197
1263506329263506330GA31GENIChomozygous108633199
1263506349263506350AG41GENIChomozygous108633200
1263506418263506419CA45GENICpossibly homozygous108633202
1263506687263506688GA56GENIChomozygous108633204
1263506819263506820TA42GENICpossibly homozygous108633206
1263506844263506845TC41GENIChomozygous108633208
1263506973263506974TC62GENIChomozygous108633210
1263507031263507032TC57GENIChomozygous108633212
1263507700263507701AG35GENIChomozygous108633214
1263507738263507739AG42GENIChomozygous108633216
1263507998263507999CT53GENICpossibly homozygous108633218
1263508005263508006CT52GENIChomozygous108633220
1263508405263508406GC57GENIChomozygous108633222
1263508558263508559TC37GENICpossibly homozygous108633224
1263509169263509170AG46GENIChomozygous108633226
1263509420263509421CA56GENIChomozygous108633228
1263509506263509507GC46GENIChomozygous108633230
1263509864263509865TC54GENIChomozygous108633232
1263509936263509937TC39GENIChomozygous108633233
1263509980263509981TC36GENIChomozygous108633235
1263510233263510234CT36GENIChomozygous108633237
1263510980263510981TC59GENIChomozygous108633239
1263511210263511211CT61GENIChomozygous108633241