[galaxy-user] intersect two file

Hello, I have a naive question. When using the "Intersect" option in "Operate on Genomic Intervals", is there an option to report the features in the second file that the feature in the first file overlaps? Currently, I am only able to get Galaxy to report that, for example, a SNP overlaps some gene (boolean yes or no), but I would really like to know __which__ gene the SNP overlaps. Help. Thanks, Aaron