| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:27217087-27217633 | Common:1; Rare:175 | ||||
| chr2:27356737-27356807 | Rare:14 | ||||
| chr2:27356943-27357199 | Common:2; Rare:94 | ||||
| chr2:27369852-27370062 | Rare:77; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:27370168-27370695 | Common:2; Rare:207 | ||||
| chr2:27380722-27380805 | Rare:31; Clinvar:2 | ||||
| chr2:27409302-27409740 | Rare:131 | ||||
| chr2:27428968-27429156 | Common:1; Rare:56 | ||||
| chr2:27433736-27434030 | Common:1; Rare:53 | ||||
| chr2:27440398-27440894 | Common:2; Rare:115 | ||||
| chr2:27582986-27583131 | Rare:53 | ||||
| chr2:27628959-27629164 | Common:1; Rare:105 | ||||
| chr2:27771657-27771812 | Common:1; Rare:58 | ||||
| chr2:27890259-27890829 | Common:2; Rare:165 | ||||
| chr2:28751508-28752165 | Common:4; Rare:258 |