| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:231680270-231680611 | Rare:61 | ||||
| chr2:231681057-231681349 | Rare:77 | ||||
| chr2:231687270-231687560 | Common:1; Rare:57 | ||||
| chr2:231701508-231701780 | Common:1; Rare:59 | ||||
| chr2:231713937-231714170 | Rare:72 | ||||
| chr2:231717326-231717575 | Common:5; Rare:45 | ||||
| chr2:231852280-231852540 | Common:1; Rare:60 | ||||
| chr2:231900580-231900741 | Common:2; Rare:29 | ||||
| chr2:231906090-231906400 | Common:3; Rare:67 | ||||
| chr2:232385670-232385900 | Common:1; Rare:51 | ||||
| chr2:232524187-232524587 | Common:2; Rare:160; Clinvar (pathogenic):2 | ||||
| chr2:232568070-232568480 | Common:1; Rare:69 | ||||
| chr2:232592812-232592927 | Common:1; Rare:19 | ||||
| chr2:232593060-232593370 | Common:4; Rare:43 | ||||
| chr2:232902077-232902218 | Rare:24 |