| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:264561-264975 | Common:4; Rare:152 | ||||
| chr2:677366-677518 | Common:1; Rare:58 | ||||
| chr2:1744511-1744668 | Common:2; Rare:56 | ||||
| chr2:3377791-3377895 | Rare:30 | ||||
| chr2:3379608-3379813 | Common:2; Rare:82 | ||||
| chr2:3519402-3519622 | Common:2; Rare:70 | ||||
| chr2:3558244-3558577 | Common:6; Rare:130 | ||||
| chr2:3575098-3575360 | Common:2; Rare:73; Clinvar:3; Clinvar (benign):5 | ||||
| chr2:8837510-8837723 | Common:1; Rare:81 | ||||
| chr2:9003955-9004055 | Rare:30 | ||||
| chr2:9423121-9423707 | Common:1; Rare:159 | ||||
| chr2:9474491-9474642 | Common:6; Rare:71 | ||||
| chr2:9555580-9555966 | Common:2; Rare:129 | ||||
| chr2:9630950-9631331 | Common:3; Rare:123 | ||||
| chr2:9843254-9843508 | Common:6; Rare:71 |