| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:27071498-27071872 | Common:1; Rare:110 | ||||
| chr2:27212223-27212376 | Common:1; Rare:81 | ||||
| chr2:27323051-27323149 | Rare:25; Clinvar (benign):1 | ||||
| chr2:27356170-27356286 | Rare:28 | ||||
| chr2:27356750-27356854 | Rare:26 | ||||
| chr2:27356961-27357071 | Rare:43 | ||||
| chr2:27370257-27370656 | Common:1; Rare:165 | ||||
| chr2:27582982-27583101 | Rare:44 | ||||
| chr2:27628981-27629064 | Common:1; Rare:41 | ||||
| chr2:27663349-27663468 | Rare:32 | ||||
| chr2:27663537-27663924 | Rare:139 | ||||
| chr2:27890402-27890809 | Rare:103 | ||||
| chr2:28751729-28752169 | Common:1; Rare:178 | ||||
| chr2:28870228-28870475 | Rare:111 | ||||
| chr2:29115347-29115636 | Common:1; Rare:78 |