| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:227717985-227718118 | Common:1; Rare:33; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:229921904-229922522 | Common:4; Rare:216 | ||||
| chr2:229922881-229923083 | Rare:48 | ||||
| chr2:229923164-229923221 | Rare:17 | ||||
| chr2:229923225-229923446 | Common:1; Rare:43 | ||||
| chr2:230219929-230220160 | Rare:34 | ||||
| chr2:230712732-230713092 | Common:5; Rare:124 | ||||
| chr2:230713597-230713667 | Rare:20 | ||||
| chr2:231460482-231460883 | Common:3; Rare:184 | ||||
| chr2:231464133-231464224 | Rare:26 | ||||
| chr2:231464337-231464700 | Common:3; Rare:127 | ||||
| chr2:231707003-231707180 | Rare:40 | ||||
| chr2:231708823-231708867 | Common:1; Rare:21 | ||||
| chr2:231710265-231710631 | Common:6; Rare:177 | ||||
| chr2:231961288-231961388 | Rare:22 |