| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:27890443-27890825 | Rare:97 | ||||
| chr2:28751499-28752127 | Common:4; Rare:254 | ||||
| chr2:28870270-28870448 | Rare:68 | ||||
| chr2:29115361-29115640 | Common:1; Rare:77 | ||||
| chr2:32039753-32039854 | Rare:30 | ||||
| chr2:32165745-32165886 | Common:1; Rare:45 | ||||
| chr2:33599222-33599618 | Common:1; Rare:139 | ||||
| chr2:37084327-37084569 | Common:3; Rare:95 | ||||
| chr2:37231542-37231712 | Common:4; Rare:99; Clinvar (benign):3 | ||||
| chr2:37324756-37324950 | Common:1; Rare:83 | ||||
| chr2:38076149-38076239 | Rare:22 | ||||
| chr2:38751335-38751616 | Common:3; Rare:132 | ||||
| chr2:38875902-38876064 | Common:1; Rare:56 | ||||
| chr2:39437090-39437453 | Common:4; Rare:128 | ||||
| chr2:42169162-42169423 | Common:1; Rare:134 |