| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:27369964-27370102 | Rare:48 | ||||
| chr2:27370272-27370685 | Common:2; Rare:169 | ||||
| chr2:27371155-27371282 | Common:1; Rare:39 | ||||
| chr2:27380386-27380666 | Common:1; Rare:99; Clinvar:5 | ||||
| chr2:27380780-27380962 | Common:1; Rare:64 | ||||
| chr2:27409372-27409803 | Rare:148 | ||||
| chr2:27429014-27429236 | Common:1; Rare:72 | ||||
| chr2:27442293-27442398 | Rare:39 | ||||
| chr2:27489618-27489975 | Common:1; Rare:93; Clinvar (benign):1 | ||||
| chr2:27537313-27537435 | Common:1; Rare:18 | ||||
| chr2:27582951-27583122 | Rare:60 | ||||
| chr2:27628856-27629133 | Common:1; Rare:127 | ||||
| chr2:27663351-27663947 | Rare:200 | ||||
| chr2:27664128-27664300 | Common:2; Rare:60 | ||||
| chr2:27664378-27664574 | Rare:66 |