chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1216869234216869235TC40GENIChomozygous108992347
1216869818216869819GC23GENIChomozygous108536171
1216869861216869862CA21GENIChomozygous108536172
1216869950216869951GA24GENIChomozygous120515512
1216869951216869952AC25GENIChomozygous120683062
1216869970216869971TC23GENIChomozygous108992349
1216877172216877173GA11GENIChomozygous109193614
1216878226216878227CT33GENIChomozygous109193616
1216878496216878497GC18GENIChomozygous120490519
1216878670216878671CG13GENIChomozygous109193618
1216881704216881705TC36GENIChomozygous108536176
1216912545216912546AG23GENIChomozygous108536183
1216914346216914347TC18GENIChomozygous108992411
1216915244216915245CA22GENIChomozygous108536188
1216915461216915462TC22GENIChomozygous108536189
1216915536216915537TG26GENIChomozygous108536190
1216916447216916448GC23GENIChomozygous108536192
1216916786216916787GA31GENIChomozygous108536193
1216916880216916881GA25GENIChomozygous108536194
1216916882216916883TC25GENIChomozygous108536195
1216916937216916938CT14GENIChomozygous108536196
1216919024216919025AG21GENIChomozygous108536198
1216919927216919928AG20GENIChomozygous108536200
1216920036216920037GA28GENIChomozygous109193620