chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4140887210140887211TG15GENIChomozygous954848418
4140887405140887406GC31GENIChomozygous954848419
4140887526140887527AG32GENIChomozygous954848420
4140888915140888916TC5GENIChomozygous954848421
4140894149140894150GA37GENIChomozygous954848422
4140894483140894484TC35GENIChomozygous954848423
4140894658140894659GC24GENIChomozygous954848424
4140896988140896989GA30GENIChomozygous954848425
4140899328140899329GA24GENIChomozygous954848426
4140901019140901020TC25GENIChomozygous954848427
4140902715140902716TC17GENIChomozygous954848428
4140902957140902958AG27GENIChomozygous954848429
4140903807140903808CT16GENIChomozygous954848430
4140906395140906396AG38GENIChomozygous954848431
4140908274140908275TG19GENIChomozygous954848432
4140908994140908995GC31GENIChomozygous954848433
4140909042140909043GA21GENIChomozygous954848434
4140909059140909060CA22GENIChomozygous954848435
4140909109140909110GA28GENIChomozygous954848436
4140909129140909130CT27GENIChomozygous954848437
4140909170140909171GA25GENIChomozygous954848438
4140909196140909197CT17GENIChomozygous954848439
4140909244140909245GT28GENIChomozygous954848440
4140909269140909270GA28GENIChomozygous954848441
4140909286140909287GC27GENIChomozygous954848442
4140913522140913523CT9GENIChomozygous954848443
4140916630140916631TG20GENIChomozygous954848444
4140916631140916632CA20GENIChomozygous954848445
4140916937140916938GA29GENIChomozygous954848446