| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:27433775-27434090 | Common:1; Rare:56 | ||||
| chr2:27442148-27442423 | Common:1; Rare:95 | ||||
| chr2:27443286-27443459 | Rare:53 | ||||
| chr2:27489643-27490123 | Common:1; Rare:127; Clinvar (benign):1 | ||||
| chr2:27496672-27496899 | Rare:43 | ||||
| chr2:27582999-27583106 | Rare:40 | ||||
| chr2:27628954-27629090 | Common:1; Rare:70 | ||||
| chr2:27663328-27663974 | Common:1; Rare:213 | ||||
| chr2:27664193-27664574 | Common:1; Rare:126 | ||||
| chr2:27771600-27772009 | Common:1; Rare:127 | ||||
| chr2:27890380-27890854 | Common:1; Rare:124 | ||||
| chr2:28392517-28392917 | Rare:136 | ||||
| chr2:28392992-28393231 | Common:1; Rare:52 | ||||
| chr2:28393318-28393826 | Common:1; Rare:141 | ||||
| chr2:28395144-28395446 | Common:6; Rare:54 |