| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:36301886-36302204 | Common:3; Rare:51 | ||||
| chr5:36876603-36876900 | Common:1; Rare:89; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:36877112-36877155 | Rare:15 | ||||
| chr5:37371053-37371178 | Rare:44 | ||||
| chr5:37379180-37379375 | Rare:52 | ||||
| chr5:38556484-38556892 | Common:3; Rare:142 | ||||
| chr5:39074346-39074505 | Common:1; Rare:71 | ||||
| chr5:39424967-39425308 | Common:3; Rare:71 | ||||
| chr5:40755780-40756097 | Rare:72 | ||||
| chr5:40798166-40798457 | Common:2; Rare:112 | ||||
| chr5:40834225-40834610 | Common:3; Rare:112 | ||||
| chr5:40835173-40835406 | Common:2; Rare:91 | ||||
| chr5:41510432-41510759 | Rare:98 | ||||
| chr5:41510780-41510807 | Common:1; Rare:3 | ||||
| chr5:41870360-41870478 | Rare:49; Clinvar:2 |