| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:14402401-14402746 | Common:4; Rare:81 | ||||
| chr3:14651474-14651836 | Rare:113 | ||||
| chr3:14947096-14947594 | Common:5; Rare:208 | ||||
| chr3:14948019-14948659 | Common:2; Rare:241 | ||||
| chr3:15065243-15065362 | Common:2; Rare:42 | ||||
| chr3:15205933-15206278 | Rare:119 | ||||
| chr3:15427401-15427629 | Common:1; Rare:71 | ||||
| chr3:15601512-15601800 | Common:4; Rare:121; Clinvar:1 | ||||
| chr3:15859777-15860127 | Common:4; Rare:112 | ||||
| chr3:16264869-16265267 | Common:3; Rare:135 | ||||
| chr3:19946974-19947409 | Common:5; Rare:161 | ||||
| chr3:20186166-20186415 | Common:2; Rare:79 | ||||
| chr3:23916902-23917208 | Rare:118 | ||||
| chr3:25783392-25783640 | Common:2; Rare:77; Clinvar (benign):3 | ||||
| chr3:28348612-28349178 | Common:3; Rare:173 |