| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:27212225-27212404 | Common:2; Rare:100 | ||||
| chr2:27217115-27217544 | Common:1; Rare:146 | ||||
| chr2:27323029-27323154 | Rare:34; Clinvar (benign):1 | ||||
| chr2:27356750-27356863 | Rare:30 | ||||
| chr2:27356973-27357193 | Common:2; Rare:79 | ||||
| chr2:27370257-27370641 | Common:1; Rare:158 | ||||
| chr2:27380517-27380901 | Common:2; Rare:140; Clinvar:7 | ||||
| chr2:27582961-27583122 | Rare:57 | ||||
| chr2:27628959-27629108 | Common:1; Rare:84 | ||||
| chr2:27663369-27663934 | Rare:186 | ||||
| chr2:27664164-27664569 | Common:2; Rare:136 | ||||
| chr2:27771602-27771775 | Common:1; Rare:63 | ||||
| chr2:27890387-27890836 | Common:1; Rare:118 | ||||
| chr2:28392633-28392863 | Rare:82 | ||||
| chr2:28395474-28395735 | Common:1; Rare:50 |