| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:178006796-178006963 | Common:2; Rare:19 | ||||
| chr5:178153788-178154170 | Rare:107; Clinvar:5; Clinvar (benign):1 | ||||
| chr5:178204339-178204534 | Common:3; Rare:68 | ||||
| chr5:178205688-178206010 | Common:1; Rare:88 | ||||
| chr5:178859797-178860114 | Common:4; Rare:93 | ||||
| chr5:178940948-178941239 | Common:1; Rare:77 | ||||
| chr5:179559534-179559814 | Common:1; Rare:79 | ||||
| chr5:179623596-179623771 | Common:1; Rare:82 | ||||
| chr5:179698575-179698605 | Rare:8 | ||||
| chr5:179698610-179699091 | Common:4; Rare:170 | ||||
| chr5:179806298-179806390 | Rare:28 | ||||
| chr5:179806890-179807063 | Common:3; Rare:62 | ||||
| chr5:179820713-179820926 | Common:6; Rare:81; Clinvar:1; Clinvar (benign):2 | ||||
| chr5:179823969-179824201 | Common:1; Rare:97; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr5:179858792-179859031 | Rare:126 |