chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
191008112310081124TC23GENIChomozygous109632242
191008536910085370GA15GENIChomozygous109632245
191008592610085927TC39GENIChomozygous109632247
191008594410085945CT39GENIChomozygous109632249
191008715610087157CG21GENIChomozygous109632251
191008739510087396CT33GENIChomozygous109632253
191008776710087768AG27GENIChomozygous109632255
191009277810092779GA25GENIChomozygous109632258
191009335810093359TC35GENIChomozygous109632261
191009352910093530CT32GENIChomozygous109632263
191009355310093554GA32GENIChomozygous109632265
191009396710093968TC36GENIChomozygous109632267
191009415210094153CT34GENIChomozygous109632269
191009443610094437AG38GENIChomozygous109632271
191009447710094478TC31GENIChomozygous109632273
191009473410094735CT24GENIChomozygous109632275
191009506110095062AG30GENIChomozygous109632277
191009509210095093TG37GENIChomozygous109632279
191009533810095339AG42GENIChomozygous109632282
191009675510096756AG23GENIChomozygous109632284
191009708910097090CT33GENIChomozygous109632286
191009764110097642CT28GENIChomozygous109632288
191009981110099812TC22GENIChomozygous109632290
191010064610100647GT32GENIChomozygous109632292
191010085810100859CT55GENIChomozygous109632294
191010105610101057CT33GENIChomozygous109632296
191009897510098976GC41GENIChomozygous109764440