chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6124125159124125161TC23GENIChomozygous137710223
6124125192124125193AG17GENIChomozygous137908351
6124125203124125204CT18GENIChomozygous137908352
6124125313124125314TA19GENIChomozygous137908353
6124125401124125401AATGGAGCT20GENIChomozygous137710224
6124125417124125418CT20GENIChomozygous137908354
6124125488124125489GA21GENIChomozygous137908355
6124125512124125513CT24GENIChomozygous137908356
6124125562124125563AG23GENIChomozygous137908357
6124125644124125644A14GENICpossibly homozygous137710225
6124125838124125839CA14GENIChomozygous137908358
6124125852124125853GT12GENIChomozygous137908359
6124126047124126053GCCTGG14GENIChomozygous137710226
6124126121124126123GT17GENIChomozygous137710227
6124126547124126548GA19GENIChomozygous137908360
6124126734124126735AG26GENIChomozygous137908361
6124127219124127220AG22GENIChomozygous137908362
6124127522124127523CT15GENIChomozygous137908363
6124128220124128221TC16GENIChomozygous137908364
6124130116124130117AG7GENIChomozygous137908365
6124127332124127333GT8GENICheterozygous148226877
6124127336124127337AT7GENICheterozygous148226878
6124127335124127335TTTTTTTTTTT9GENICheterozygous148225996