chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
97960381879603818TG14GENIChomozygous128726870
97960382279603822TATTTGTTTTGGTGTTGTTGGGTTTTTTGGGGGGTGTGGGG14GENIChomozygous128726871
97960473579604736G7GENIChomozygous128726872
97960474179604742T6GENIChomozygous128726873
97960475179604752G6GENIChomozygous128726874
97960475379604754G6GENIChomozygous128726875
97960475679604757C6GENIChomozygous128726876
97960476479604765G6GENIChomozygous128726877
97960476779604768AG6GENIChomozygous117380740
97960477679604777G4GENIChomozygous128726878
97962130679621307TA21GENIChomozygous117380743
97962130779621308TG21GENIChomozygous117380744