chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4122125358122125359AT28GENICheterozygous112825144
4122125452122125453GC31GENICheterozygous112825148
4122125477122125478CT28GENICheterozygous112825150
4122125483122125484TG26GENICheterozygous112825152
4122125497122125498AC28GENICheterozygous112825154
4122125744122125745AT26GENICheterozygous112825158
4122125771122125772AT30GENICheterozygous112825160
4122125824122125825AG34GENICheterozygous113155260
4122126059122126060AT27GENICheterozygous113049186
4122127161122127162TA23GENICheterozygous112825166
4122127195122127196AC23GENICheterozygous112825168
4122127202122127203CG24GENICheterozygous112825170
4122130445122130446AC2GENIChomozygous112825172
4122130745122130746TC18GENICheterozygous112825177
4122130793122130794GT19GENICheterozygous112825179
4122130801122130802TC19GENICheterozygous112825181
4122130839122130840AC37GENICheterozygous112825183
4122130852122130853GA41GENICheterozygous112825185
4122130863122130864TC48GENICheterozygous112825187
4122130898122130899TC50GENICheterozygous112825189
4122130900122130901TC48GENICheterozygous112825191
4122130932122130933CT48GENICheterozygous112825193
4122130975122130976AG43GENICheterozygous112825195
4122131039122131040CT40GENICheterozygous112825197
4122131044122131045CG42GENICheterozygous112825199
4122131106122131107GT55GENICheterozygous112825201
4122131164122131165TC47GENICheterozygous112825203
4122131193122131194TC36GENICheterozygous112825205
4122131218122131219AG36GENICheterozygous112825207
4122131326122131327AT44GENICheterozygous112825209
4122131343122131344GA43GENICheterozygous112825211
4122131385122131386GC52GENICheterozygous112825213
4122131388122131389AG49GENICheterozygous112825215
4122131447122131448GA57GENICheterozygous112825217
4122131462122131463CG61GENICheterozygous112825219
4122131510122131511TG48GENICheterozygous112825223
4122126043122126044CT21GENICheterozygous113241082
4122126038122126039CT21GENICheterozygous113241081