chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4140887210140887211TG28GENIChomozygous793689193
4140887405140887406GC49GENICpossibly homozygous793689194
4140887526140887527AG35GENIChomozygous793689195
4140889290140889291CA46GENICpossibly homozygous793689196
4140892114140892115TA38GENIChomozygous793689197
4140894149140894150GA45GENIChomozygous793689198
4140894483140894484TC29GENIChomozygous793689199
4140894658140894659GC25GENIChomozygous793689200
4140896988140896989GA28GENIChomozygous793689201
4140899328140899329GA27GENIChomozygous793689202
4140901019140901020TC26GENICpossibly homozygous793689203
4140902715140902716TC26GENIChomozygous793689204
4140902957140902958AG35GENIChomozygous793689205
4140903807140903808CT58GENIChomozygous793689206
4140904293140904294CG7GENIChomozygous793689207
4140904305140904306TC3GENIChomozygous793689208
4140906395140906396AG44GENIChomozygous793689209
4140907673140907674TC26GENICheterozygous793689210
4140908274140908275TG35GENIChomozygous793689211
4140908994140908995GC35GENIChomozygous793689212
4140909042140909043GA47GENIChomozygous793689213
4140909059140909060CA45GENIChomozygous793689214
4140909109140909110GA45GENIChomozygous793689215
4140909129140909130CT48GENICpossibly homozygous793689216
4140909170140909171GA43GENIChomozygous793689217
4140909196140909197CT41GENIChomozygous793689218
4140909244140909245GT36GENIChomozygous793689219
4140909248140909249TA38GENIChomozygous793689220
4140909269140909270GA39GENIChomozygous793689221
4140909286140909287GC40GENIChomozygous793689222
4140913023140913024AG39GENIChomozygous793689223
4140913522140913523CT20GENIChomozygous793689224
4140916630140916631TG37GENIChomozygous793689225
4140916631140916632CA37GENIChomozygous793689226
4140916937140916938GA32GENIChomozygous793689227