| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:27323043-27323155 | Rare:27; Clinvar (benign):1 | ||||
| chr2:27356750-27357191 | Common:2; Rare:132 | ||||
| chr2:27370257-27370738 | Common:2; Rare:199 | ||||
| chr2:27582959-27583117 | Rare:56 | ||||
| chr2:27628954-27629073 | Common:1; Rare:57 | ||||
| chr2:27663369-27663467 | Rare:28 | ||||
| chr2:27663545-27663911 | Rare:131 | ||||
| chr2:27771667-27772016 | Common:1; Rare:108 | ||||
| chr2:27890394-27890788 | Rare:100 | ||||
| chr2:28392502-28392858 | Rare:118 | ||||
| chr2:28395473-28395735 | Common:1; Rare:50 | ||||
| chr2:28630492-28630590 | Common:1; Rare:43 | ||||
| chr2:28751682-28752406 | Common:3; Rare:289 | ||||
| chr2:28870262-28870454 | Rare:75 | ||||
| chr2:28894487-28894717 | Rare:85 |