Aromatic compounds display several absorbances in the fingerprint region that can be useful as structural identifiers, particularly with regard to substitution patterns. These generally arise from out-of-plane C-H bending motions, and the frequencies indicate the number of adjacent hydrogens:

Obviously, in something like a meta-disubstituted ring, there will be a combination of bands, while in a para-disubstituted ring, there will be only one. There are also ring deformations that crop up in to 600-900 cm^-1, so one normally looks for characteristic patters.