| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:177303693-177304053 | Common:3; Rare:137 | ||||
| chr5:177351643-177351688 | Rare:12 | ||||
| chr5:177371031-177371105 | Common:18; Rare:75 | ||||
| chr5:177497542-177497865 | Common:1; Rare:118 | ||||
| chr5:177516889-177517079 | Common:2; Rare:76; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr5:177592069-177592212 | Common:1; Rare:53 | ||||
| chr5:179559560-179559781 | Common:1; Rare:62 | ||||
| chr5:179623616-179623988 | Common:4; Rare:135 | ||||
| chr5:179698692-179699091 | Common:3; Rare:128 | ||||
| chr5:180330903-180331140 | Common:3; Rare:48 | ||||
| chr5:180353325-180353513 | Common:5; Rare:76 | ||||
| chr5:180861150-180861394 | Common:2; Rare:98 | ||||
| chr5:181223118-181223313 | Rare:66 | ||||
| chr5:181261086-181261239 | Rare:52 | ||||
| chr6:3258797-3259020 | Rare:85 |