chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
727555192755519A10GENICpossibly homozygous128432345
727570062757007TC21GENIChomozygous115545778
727589722758973GC16GENIChomozygous115545780
727600232760026TTA12GENIChomozygous128432346
727613552761356TC12GENIChomozygous115545782
727628332762834AG18GENIChomozygous115545785
727642882764289CA28GENIChomozygous115545787
727659672765984ATGTCAGCATGGACAGC15GENIChomozygous128432347
727616312761632T20GENICheterozygous131673673
727680282768030TC7GENIChomozygous131870056
727680312768063GCATGGACAGTATGACAGCATGGACAGTATGT9GENICpossibly homozygous131870057
727687442768745CT17GENIChomozygous115545849
727695302769531GT27GENIChomozygous115545851
727705122770512T13GENIChomozygous128432348
727730362773036ACATACAT13GENIChomozygous128432349
727731862773196ACATATATAC22GENIChomozygous128432350
727743832774384AG11GENIChomozygous115545853
727746772774678AG12GENIChomozygous115545855
727747012774702AG12GENIChomozygous115545857
727747142774715CT12GENIChomozygous115545860
727781742778175TC22GENIChomozygous115545862
727783912778392TC16GENIChomozygous115545864
727784332778434TA19GENIChomozygous115545866
727785222778523TC17GENIChomozygous115545869
727787232778724AG13GENIChomozygous115545871