chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5166430482166430483TC24GENICpossibly homozygous57303044
5166430737166430738AG34GENICpossibly homozygous56079148
5166432070166432071TG9GENIChomozygous56079155
5166433241166433242CT9INTERGENICpossibly homozygous57303047
5166435040166435041A-6INTERGENICheterozygous56079169
5166435456166435457CT18INTERGENICpossibly homozygous56079171
5166440480166440481GA13INTERGENIChomozygous56079173
5166440693166440694G-7INTERGENIChomozygous56079174
5166440707166440708TC10INTERGENIChomozygous56831098
5166440763166440764TG25INTERGENICpossibly homozygous56079176
5166440885166440886GT22INTERGENIChomozygous56079177
5166441145166441146TG16INTERGENIChomozygous56079178
5166441468166441469AG26INTERGENICpossibly homozygous56079179
5166441881166441882CT11INTERGENICpossibly homozygous56079180
5166442321166442322CG13INTERGENIChomozygous57303053
5166442378166442379GA22INTERGENIChomozygous57303056
5166442498166442499TC20INTERGENICpossibly homozygous56079181
5166442542166442543AC15INTERGENICpossibly homozygous56079182
5166443041166443042TC16INTERGENICpossibly homozygous57303062