chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7130430686130430687TG13GENIChomozygous950231258
7130432419130432420CA11GENICpossibly homozygous950231259
7130433453130433454CA26GENIChomozygous950231260
7130434093130434094AT6GENIChomozygous950231261
7130435479130435480AG6GENIChomozygous950231262
7130435663130435664GT10GENIChomozygous950231263
7130435821130435822TC10GENIChomozygous950231264
7130436509130436510AG12GENIChomozygous950231265
7130436753130436754CT14GENIChomozygous950231266
7130436895130436896AG15GENIChomozygous950231267
7130436928130436929AG14GENIChomozygous950231268
7130438990130438991GA10GENICpossibly homozygous950231269
7130439433130439434GA18GENIChomozygous950231270
7130439443130439444TC19GENIChomozygous950231271