| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:10307750-10308190 | Common:4; Rare:84 | ||||
| chr5:10353448-10353920 | Common:4; Rare:165 | ||||
| chr5:10441779-10441937 | Rare:42 | ||||
| chr5:10564134-10564391 | Common:2; Rare:82 | ||||
| chr5:10761197-10761519 | Common:13; Rare:91 | ||||
| chr5:11385904-11386304 | Common:6; Rare:121 | ||||
| chr5:11588934-11589241 | Common:1; Rare:67 | ||||
| chr5:11904367-11904706 | Rare:70 | ||||
| chr5:14143068-14143364 | Rare:99 | ||||
| chr5:14387218-14387882 | Common:6; Rare:209 | ||||
| chr5:14581633-14581869 | Rare:106 | ||||
| chr5:14664400-14664671 | Common:3; Rare:102 | ||||
| chr5:14871670-14872050 | Common:3; Rare:107; Clinvar (benign):1 | ||||
| chr5:15499969-15500220 | Common:2; Rare:83 | ||||
| chr5:15501534-15501701 | Rare:29 |