| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:27217296-27217494 | Rare:83 | ||||
| chr2:27263031-27263181 | Rare:38 | ||||
| chr2:27323029-27323154 | Rare:34; Clinvar (benign):1 | ||||
| chr2:27356746-27357067 | Rare:90 | ||||
| chr2:27370275-27370641 | Common:1; Rare:151 | ||||
| chr2:27582810-27583101 | Rare:98 | ||||
| chr2:27628981-27629098 | Common:1; Rare:64 | ||||
| chr2:27663369-27663467 | Rare:28 | ||||
| chr2:27663533-27663927 | Rare:140 | ||||
| chr2:27890447-27890812 | Rare:94 | ||||
| chr2:28751720-28752134 | Common:2; Rare:171 | ||||
| chr2:28870267-28870475 | Rare:81 | ||||
| chr2:32010260-32010361 | Rare:23 | ||||
| chr2:32039747-32039851 | Rare:34 | ||||
| chr2:32165737-32165886 | Common:1; Rare:49 |