chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7130430686130430687TG13GENIChomozygous115890200
7130432419130432420CA11GENICpossibly homozygous115890204
7130433453130433454CA26GENIChomozygous115890206
7130434093130434094AT6GENIChomozygous116346162
7130435479130435480AG6GENIChomozygous115890208
7130435663130435664GT10GENIChomozygous116346164
7130435821130435822TC10GENIChomozygous115890212
7130436509130436510AG12GENIChomozygous115890214
7130436753130436754CT14GENIChomozygous115890216
7130436895130436896AG15GENIChomozygous115890218
7130436928130436929AG14GENIChomozygous115890220
7130438990130438991GA10GENICpossibly homozygous116346166
7130439433130439434GA18GENIChomozygous116346168
7130439443130439444TC19GENIChomozygous115890222