| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:197736877-197737185 | Common:3; Rare:100 | ||||
| chr3:197749826-197749957 | Rare:55 | ||||
| chr3:197949894-197950243 | Common:4; Rare:106; Clinvar (benign):2 | ||||
| chr4:337468-337843 | Common:1; Rare:103 | ||||
| chr4:499147-499324 | Common:2; Rare:62 | ||||
| chr4:673872-673977 | Rare:46 | ||||
| chr4:674212-674614 | Common:4; Rare:185 | ||||
| chr4:932264-932487 | Common:2; Rare:87 | ||||
| chr4:1712310-1712396 | Common:1; Rare:28 | ||||
| chr4:1721205-1721512 | Common:2; Rare:94 | ||||
| chr4:2041911-2042068 | Common:1; Rare:61 | ||||
| chr4:2468927-2469163 | Common:1; Rare:78 | ||||
| chr4:2843709-2844009 | Common:3; Rare:107 | ||||
| chr4:2934777-2934889 | Common:1; Rare:53 | ||||
| chr4:2963327-2963629 | Common:3; Rare:109 |