chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
123931530439315305TC18GENIChomozygous639170303
123931561239315613GC27GENIChomozygous639170304
123931573739315738GGTAT26GENIChomozygous750512176
123931578939315790T-18GENIChomozygous750512177
123931773439317735CT21GENIChomozygous639170305
123931785439317855TC22GENIChomozygous639170306
123932172439321725AG28GENIChomozygous639170307
123932194939321950CT27GENIChomozygous639170308
123932264839322649CG21GENIChomozygous639170309
123932270639322707CT17GENICheterozygous639170310
123932321339323214TC34GENIChomozygous639170311