| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:27489634-27490039 | Common:2; Rare:201; Clinvar (benign):2 | ||||
| chr2:27582947-27583125 | Rare:115 | ||||
| chr2:27628901-27629132 | Common:3; Rare:271 | ||||
| chr2:27663332-27663993 | Common:2; Rare:547 | ||||
| chr2:27771562-27771828 | Common:3; Rare:218 | ||||
| chr2:27771830-27772080 | Rare:78 | ||||
| chr2:27890314-27890958 | Common:4; Rare:428 | ||||
| chr2:28392071-28392493 | Common:4; Rare:196 | ||||
| chr2:28392496-28393134 | Common:1; Rare:383 | ||||
| chr2:28393225-28393823 | Common:1; Rare:164 | ||||
| chr2:28751430-28752179 | Common:11; Rare:831 | ||||
| chr2:28810510-28810990 | Common:1; Rare:106 | ||||
| chr2:28870194-28870519 | Rare:335 | ||||
| chr2:28894353-28894858 | Common:10; Rare:417 | ||||
| chr2:28895258-28895948 | Common:10; Rare:422 |