chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5166430482166430483TC17GENIChomozygous57303044
5166430737166430738AG21GENIChomozygous56079148
5166432070166432071TG18GENICpossibly homozygous56079155
5166433241166433242CT21INTERGENIChomozygous57303047
5166434561166434563CT--19INTERGENICpossibly homozygous57303050
5166435040166435041A-18INTERGENIChomozygous56079169
5166435456166435457CT31INTERGENIChomozygous56079171
5166440480166440481GA27INTERGENICpossibly homozygous56079173
5166440693166440694G-25INTERGENIChomozygous56079174
5166440707166440708TC24INTERGENIChomozygous56831098
5166440763166440764TG28INTERGENIChomozygous56079176
5166440885166440886GT37INTERGENIChomozygous56079177
5166441145166441146TG30INTERGENIChomozygous56079178
5166441468166441469AG26INTERGENICpossibly homozygous56079179
5166441881166441882CT17INTERGENIChomozygous56079180
5166442321166442322CG25INTERGENIChomozygous57303053
5166442378166442379GA21INTERGENIChomozygous57303056
5166442498166442499TC26INTERGENIChomozygous56079181
5166442542166442543AC32INTERGENIChomozygous56079182
5166442879166442880TTTCTGTGTGTGTG3INTERGENIChomozygous57303059
5166443041166443042TC27INTERGENIChomozygous57303062