Calculated data indicating that the form of the HOMA geometric aromaticity index is universal and allows the design of electronic and magnetic descriptors

Raw computational data for the carbocyclic structures presented in Figure 1 of J. Org. Chem. 90(2025)8674 manuscript. All calculations were carried out with Gaussian 16 using the B3LYP, TPSSh, and ωB97X-D methods together with the D3 dispersion correction and aug-cc-pvtz basis set. The data