| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:27032867-27033011 | Rare:54 | ||||
| chr2:27071498-27071898 | Common:1; Rare:118 | ||||
| chr2:27086606-27086801 | Common:1; Rare:54; Clinvar (benign):1 | ||||
| chr2:27211747-27212127 | Common:3; Rare:129 | ||||
| chr2:27212223-27212375 | Common:1; Rare:80 | ||||
| chr2:27217115-27217461 | Common:1; Rare:113 | ||||
| chr2:27323029-27323150 | Rare:34; Clinvar (benign):1 | ||||
| chr2:27356151-27356286 | Rare:30 | ||||
| chr2:27356738-27357170 | Common:2; Rare:124 | ||||
| chr2:27370238-27370746 | Common:2; Rare:208 | ||||
| chr2:27380762-27380908 | Common:1; Rare:45 | ||||
| chr2:27442218-27442428 | Rare:78 | ||||
| chr2:27582932-27583106 | Rare:65 | ||||
| chr2:27628934-27629108 | Common:1; Rare:94 | ||||
| chr2:27663369-27663938 | Rare:189 |