| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:196318179-196318342 | Common:1; Rare:71 | ||||
| chr3:196432395-196432624 | Common:1; Rare:93 | ||||
| chr3:196639471-196639785 | Common:2; Rare:74 | ||||
| chr3:196867748-196867988 | Rare:87 | ||||
| chr3:196942395-196942682 | Common:1; Rare:117 | ||||
| chr3:197029779-197029938 | Common:1; Rare:51 | ||||
| chr3:197736841-197737207 | Common:3; Rare:122 | ||||
| chr3:197749825-197750031 | Rare:80 | ||||
| chr3:197949894-197950240 | Common:4; Rare:106; Clinvar (benign):2 | ||||
| chr3:197950836-197950978 | Rare:35; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:197959989-197960259 | Common:1; Rare:94 | ||||
| chr4:499141-499335 | Common:2; Rare:75 | ||||
| chr4:674210-674552 | Common:2; Rare:157 | ||||
| chr4:932250-932487 | Common:2; Rare:93 | ||||
| chr4:1113524-1113630 | Common:2; Rare:38 |