chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2039956323995633GA16INTERGENICheterozygous45374463
2039957573995758AC13INTERGENICheterozygous45730052
2039957743995775AG12INTERGENIChomozygous45374464
2039963743996375GA11GENICheterozygous45374465
2039964713996472TG9GENIChomozygous45374466
2039968303996831CG11GENICheterozygous45730053
2039968593996860GGCA10GENICheterozygous45730054
2039984433998444GA7GENICheterozygous45730056
2039987603998761AG7GENIChomozygous45374475
2039988943998895GGAA8GENICheterozygous45838316
2039991353999136CT15GENICheterozygous45730057
2039999503999951TTA13GENICheterozygous45730058
2040013684001369AG9GENICheterozygous45374476
2040016014001602GC13GENICheterozygous45730059
2040018874001888A-8GENICheterozygous45374477
2040025324002533AG13GENIChomozygous45374478
2040026384002639TA14GENICheterozygous45374479
2040030864003087CT7GENIChomozygous45374480
2040045894004590GA10GENICheterozygous45374487
2040047554004756TG13GENIChomozygous45374488
2040047564004757CA12GENIChomozygous45374489
2040047634004764CT14GENIChomozygous45374490
2040054344005435CT13GENICheterozygous45730062
2040062174006218AG9GENIChomozygous45374494
2040064404006441AG17GENIChomozygous45374495
2040076284007629AC8GENIChomozygous45374498
2040082944008295CT8GENIChomozygous45374499
2040093984009399G-12GENIChomozygous45374500