| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:27078526-27078723 | Common:2; Rare:49 | ||||
| chr2:27211730-27212088 | Common:3; Rare:122 | ||||
| chr2:27212252-27212371 | Common:1; Rare:59 | ||||
| chr2:27217215-27217398 | Rare:65 | ||||
| chr2:27323058-27323162 | Rare:28 | ||||
| chr2:27356750-27357087 | Rare:94 | ||||
| chr2:27370310-27370633 | Common:1; Rare:127 | ||||
| chr2:27489662-27489968 | Common:1; Rare:76; Clinvar (benign):1 | ||||
| chr2:27582973-27583106 | Rare:50 | ||||
| chr2:27628959-27629058 | Common:1; Rare:51 | ||||
| chr2:27663369-27663467 | Rare:28 | ||||
| chr2:27663505-27663911 | Rare:137 | ||||
| chr2:27771639-27772009 | Common:1; Rare:115 | ||||
| chr2:27890394-27890825 | Rare:111 | ||||
| chr2:28751694-28752134 | Common:2; Rare:188 |