| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:13480040-13480330 | Common:2; Rare:67 | ||||
| chr3:14124685-14125190 | Common:4; Rare:148; Clinvar:5; Clinvar (benign):1 | ||||
| chr3:14178530-14178888 | Common:2; Rare:189; Clinvar:5; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:14402437-14402722 | Rare:65 | ||||
| chr3:14651457-14651828 | Rare:110 | ||||
| chr3:14947244-14947563 | Common:3; Rare:146 | ||||
| chr3:14948422-14948637 | Common:2; Rare:62 | ||||
| chr3:15099119-15099256 | Rare:32 | ||||
| chr3:15206069-15206274 | Rare:80 | ||||
| chr3:15427465-15427786 | Common:2; Rare:108 | ||||
| chr3:15601478-15601810 | Common:4; Rare:141; Clinvar:2 | ||||
| chr3:15601859-15602042 | Common:1; Rare:94; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr3:15859782-15860114 | Common:4; Rare:104 | ||||
| chr3:16264872-16265243 | Common:2; Rare:124 | ||||
| chr3:17742513-17742963 | Common:4; Rare:161 |