| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:179698610-179699099 | Common:4; Rare:174 | ||||
| chr5:179820773-179821098 | Common:3; Rare:125; Clinvar:6; Clinvar (benign):2 | ||||
| chr5:179821102-179821138 | Common:1; Rare:13; Clinvar:1; Clinvar (benign):2 | ||||
| chr5:179823908-179824239 | Common:1; Rare:132; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr5:179858797-179858993 | Rare:108 | ||||
| chr5:180291892-180292197 | Common:2; Rare:112 | ||||
| chr5:180353306-180353512 | Common:6; Rare:93 | ||||
| chr5:180802756-180802976 | Common:8; Rare:86 | ||||
| chr5:180810108-180810229 | Common:1; Rare:27 | ||||
| chr5:181223131-181223313 | Rare:62 | ||||
| chr5:181223504-181223729 | Common:3; Rare:57 | ||||
| chr5:181243690-181243875 | Common:2; Rare:58 | ||||
| chr5:181261081-181261290 | Rare:71 | ||||
| chr6:292414-292537 | Rare:36 | ||||
| chr6:693074-693194 | Rare:38 |