| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:155870292-155870764 | Common:2; Rare:135 | ||||
| chr3:156674343-156674784 | Common:4; Rare:122 | ||||
| chr3:156826129-156826323 | Common:3; Rare:59 | ||||
| chr3:157159843-157160344 | Common:1; Rare:189 | ||||
| chr3:157436845-157436870 | Rare:9 | ||||
| chr3:158105732-158105893 | Common:5; Rare:80; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:158672560-158672852 | Common:4; Rare:72 | ||||
| chr3:158732153-158732499 | Common:10; Rare:124 | ||||
| chr3:158732777-158732848 | Rare:11 | ||||
| chr3:158801980-158802192 | Common:2; Rare:94 | ||||
| chr3:159763128-159763220 | Rare:23 | ||||
| chr3:159763616-159763759 | Rare:42 | ||||
| chr3:159764282-159764594 | Common:2; Rare:90 | ||||
| chr3:159852997-159853295 | Rare:50 | ||||
| chr3:160399175-160399656 | Rare:131; Clinvar:7 |