| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:27356636-27357271 | Common:3; Rare:190 | ||||
| chr2:27370189-27370707 | Common:2; Rare:205 | ||||
| chr2:27379702-27380013 | Common:3; Rare:67 | ||||
| chr2:27380547-27380994 | Common:2; Rare:166; Clinvar:7 | ||||
| chr2:27408804-27409081 | Rare:57 | ||||
| chr2:27409198-27409333 | Common:1; Rare:36 | ||||
| chr2:27409471-27409854 | Rare:132 | ||||
| chr2:27428363-27428734 | Common:1; Rare:135 | ||||
| chr2:27428968-27429287 | Common:3; Rare:91 | ||||
| chr2:27429376-27429503 | Rare:24 | ||||
| chr2:27489656-27490035 | Common:1; Rare:95; Clinvar (benign):1 | ||||
| chr2:27582756-27583245 | Rare:155 | ||||
| chr2:27628864-27629132 | Common:1; Rare:125 | ||||
| chr2:27663365-27663451 | Rare:24 | ||||
| chr2:27663474-27663993 | Common:1; Rare:183 |