| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:197029779-197029938 | Common:1; Rare:51 | ||||
| chr3:197736847-197737214 | Common:3; Rare:121 | ||||
| chr3:197749831-197749984 | Rare:65 | ||||
| chr3:197791196-197791281 | Common:1; Rare:36 | ||||
| chr3:197949861-197950315 | Common:4; Rare:133; Clinvar (benign):2 | ||||
| chr3:197950497-197950759 | Rare:68 | ||||
| chr3:197950827-197950978 | Rare:37; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:197959968-197960250 | Common:1; Rare:99 | ||||
| chr4:53073-53404 | Rare:5 | ||||
| chr4:124279-124543 | Common:6; Rare:75 | ||||
| chr4:337544-337932 | Common:5; Rare:106 | ||||
| chr4:499124-499333 | Common:3; Rare:84 | ||||
| chr4:673842-673975 | Rare:53 | ||||
| chr4:674212-674623 | Common:4; Rare:187 | ||||
| chr4:681157-681225 | Rare:22 |