chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7130430686130430687TG14GENIChomozygous982618722
7130432419130432420CA19GENICpossibly homozygous982618723
7130433453130433454CA24GENIChomozygous982618724
7130435479130435480AG12GENIChomozygous982618725
7130435663130435664GC8GENIChomozygous982618726
7130435821130435822TC9GENIChomozygous982618727
7130436509130436510AG23GENIChomozygous982618728
7130436753130436754CT29GENIChomozygous982618729
7130436895130436896AG26GENIChomozygous982618730
7130436928130436929AG32GENIChomozygous982618731
7130439443130439444TC19GENIChomozygous982618732
7130439815130439816GA16GENIChomozygous982618733