chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4140887210140887211TG9GENIChomozygous889169473
4140887405140887406GC16GENIChomozygous889169474
4140887526140887527AG11GENIChomozygous889169475
4140889290140889291CA5GENIChomozygous889169476
4140892114140892115TA10GENIChomozygous889169477
4140894149140894150GA22GENIChomozygous889169478
4140894483140894484TC14GENIChomozygous889169479
4140894658140894659GC13GENIChomozygous889169480
4140896988140896989GA23GENIChomozygous889169481
4140899328140899329GA21GENIChomozygous889169482
4140903807140903808CT7GENIChomozygous889169483
4140907775140907776TG6GENIChomozygous889169484
4140908274140908275TG9GENIChomozygous889169485
4140908994140908995GC15GENIChomozygous889169486
4140909042140909043GA15GENIChomozygous889169487
4140909059140909060CA17GENIChomozygous889169488
4140909109140909110GA7GENIChomozygous889169489
4140909196140909197CT12GENIChomozygous889169490
4140909244140909245GT10GENIChomozygous889169491
4140909248140909249TA8GENICheterozygous889169492
4140909269140909270GA10GENIChomozygous889169493
4140909286140909287GC19GENIChomozygous889169494
4140916630140916631TG5GENIChomozygous889169495
4140916631140916632CA4GENIChomozygous889169496
4140916937140916938GA16GENIChomozygous889169497