chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7130430686130430687TG42INTERGENIChomozygous808124848
7130431011130431012GC9INTERGENIChomozygous808124849
7130432419130432420CA52GENICpossibly homozygous808124850
7130433453130433454CA46GENIChomozygous808124851
7130435479130435480AG48GENIChomozygous808124852
7130435663130435664GC35GENIChomozygous808124853
7130435821130435822TC49GENICpossibly homozygous808124854
7130436509130436510AG51GENIChomozygous808124855
7130436753130436754CT64GENIChomozygous808124856
7130436895130436896AG42GENIChomozygous808124857
7130436928130436929AG43GENIChomozygous808124858
7130439443130439444TC53GENIChomozygous808124859
7130439815130439816GA48GENICpossibly homozygous808124860