| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:28241472-28241783 | Common:2; Rare:109 | ||||
| chr3:28348592-28348747 | Rare:35 | ||||
| chr3:28348779-28349227 | Common:4; Rare:143 | ||||
| chr3:28510884-28511032 | Common:1; Rare:29 | ||||
| chr3:29280837-29281081 | Common:3; Rare:49 | ||||
| chr3:29281321-29281367 | Common:1; Rare:7 | ||||
| chr3:31532084-31532172 | Common:2; Rare:24 | ||||
| chr3:31532371-31532752 | Common:4; Rare:115 | ||||
| chr3:31533395-31533507 | Rare:40 | ||||
| chr3:31703695-31704022 | Common:2; Rare:58 | ||||
| chr3:31704293-31704309 | Rare:6 | ||||
| chr3:31709130-31709300 | Rare:46 | ||||
| chr3:31906974-31907099 | Rare:19 | ||||
| chr3:31981488-31981808 | Common:2; Rare:66 | ||||
| chr3:32106410-32106697 | Common:4; Rare:79; Clinvar:2; Clinvar (benign):1 |