| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:196712228-196712574 | Common:5; Rare:110 | ||||
| chr3:196739817-196740115 | Common:2; Rare:105 | ||||
| chr3:196867748-196867967 | Rare:80 | ||||
| chr3:196942388-196942869 | Common:1; Rare:207 | ||||
| chr3:197029779-197029902 | Common:1; Rare:41 | ||||
| chr3:197736838-197737148 | Common:3; Rare:103 | ||||
| chr3:197749821-197749974 | Rare:65 | ||||
| chr3:197949886-197950260 | Common:4; Rare:112; Clinvar (benign):2 | ||||
| chr3:197959926-197960245 | Common:1; Rare:106 | ||||
| chr4:337488-337873 | Common:2; Rare:109 | ||||
| chr4:499123-499340 | Common:3; Rare:90 | ||||
| chr4:663652-663748 | Rare:31 | ||||
| chr4:673832-673952 | Rare:50 | ||||
| chr4:674228-674616 | Common:3; Rare:180 | ||||
| chr4:687576-687754 | Rare:55 |