| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:27409485-27409861 | Rare:130 | ||||
| chr2:27428229-27428339 | Common:1; Rare:19 | ||||
| chr2:27428415-27428765 | Common:1; Rare:135 | ||||
| chr2:27428939-27429250 | Common:1; Rare:90 | ||||
| chr2:27489685-27490123 | Common:1; Rare:111; Clinvar (benign):1 | ||||
| chr2:27495165-27495301 | Rare:44 | ||||
| chr2:27582736-27583213 | Rare:154 | ||||
| chr2:27628124-27628254 | Common:2; Rare:28 | ||||
| chr2:27628859-27629132 | Common:1; Rare:126 | ||||
| chr2:27663493-27664002 | Common:1; Rare:181 | ||||
| chr2:27771535-27771812 | Common:1; Rare:92 | ||||
| chr2:27771924-27771995 | Rare:21 | ||||
| chr2:27890444-27890854 | Rare:105 | ||||
| chr2:27890965-27891034 | Rare:14 | ||||
| chr2:27891112-27891350 | Rare:45 |