| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:27356750-27356855 | Rare:27 | ||||
| chr2:27356979-27357191 | Common:2; Rare:78 | ||||
| chr2:27370247-27370674 | Common:1; Rare:173 | ||||
| chr2:27371074-27371317 | Common:1; Rare:72 | ||||
| chr2:27380542-27380900 | Common:2; Rare:133; Clinvar:7 | ||||
| chr2:27442218-27442392 | Rare:56 | ||||
| chr2:27489651-27490006 | Common:1; Rare:90; Clinvar (benign):1 | ||||
| chr2:27582997-27583101 | Rare:40 | ||||
| chr2:27628970-27629091 | Common:1; Rare:64 | ||||
| chr2:27663349-27663472 | Rare:33 | ||||
| chr2:27663501-27663941 | Rare:156 | ||||
| chr2:27771607-27772045 | Common:1; Rare:138 | ||||
| chr2:27772254-27772325 | Rare:7 | ||||
| chr2:27890387-27890822 | Common:1; Rare:113 | ||||
| chr2:27891095-27891374 | Rare:51 |