| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:196942388-196942686 | Common:1; Rare:124 | ||||
| chr3:197298582-197298723 | Rare:43 | ||||
| chr3:197736846-197737221 | Common:3; Rare:124 | ||||
| chr3:197749829-197749995 | Rare:69 | ||||
| chr3:197791111-197791327 | Common:2; Rare:86 | ||||
| chr3:197858798-197858874 | Common:1; Rare:26 | ||||
| chr3:197949876-197950328 | Common:4; Rare:131; Clinvar (benign):2 | ||||
| chr3:197950822-197950978 | Rare:39; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:197960070-197960242 | Common:1; Rare:69 | ||||
| chr4:337544-337879 | Common:3; Rare:93 | ||||
| chr4:499141-499335 | Common:2; Rare:75 | ||||
| chr4:663592-663725 | Rare:42 | ||||
| chr4:674210-674521 | Common:1; Rare:139 | ||||
| chr4:932250-932481 | Common:2; Rare:90 | ||||
| chr4:1113524-1113647 | Common:2; Rare:47 |