chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4163130352163130353G5GENIChomozygous128099483
4163130363163130363C7GENIChomozygous128099484
4163130367163130368G7GENIChomozygous128099485
4163130372163130373T7GENIChomozygous128099486
4163130386163130388AG8GENIChomozygous128099487
4163130408163130408A11GENIChomozygous128099488
4163130416163130416T13GENIChomozygous128099489
4163130419163130420C14GENIChomozygous128099490
4163130426163130426A16GENIChomozygous128099491
4163130456163130456A20GENIChomozygous130299428
4163130475163130476TG19GENIChomozygous112921863
4163130496163130496A17GENIChomozygous130299429
4163130501163130501G17GENIChomozygous130299430
4163130504163130504C17GENIChomozygous130299431
4163130508163130509TG17GENIChomozygous112921865
4163130527163130529GC15GENIChomozygous130299432