| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:27428960-27429240 | Common:2; Rare:158 | ||||
| chr2:27489669-27490001 | Common:2; Rare:160; Clinvar (benign):2 | ||||
| chr2:27582797-27583121 | Rare:157 | ||||
| chr2:27583160-27583320 | Rare:69 | ||||
| chr2:27628982-27629106 | Common:2; Rare:117 | ||||
| chr2:27663332-27663938 | Rare:367 | ||||
| chr2:27771628-27771810 | Common:2; Rare:120 | ||||
| chr2:27890341-27890841 | Common:2; Rare:272 | ||||
| chr2:27891093-27891348 | Rare:93 | ||||
| chr2:28392679-28393080 | Common:2; Rare:245 | ||||
| chr2:28393126-28393624 | Rare:243 | ||||
| chr2:28395398-28395798 | Common:3; Rare:122 | ||||
| chr2:28751464-28752285 | Common:9; Rare:591 | ||||
| chr2:28870218-28870483 | Rare:201 | ||||
| chr2:28894300-28894756 | Common:10; Rare:289 |