| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:130746786-130746935 | Common:3; Rare:44 | ||||
| chr3:130893905-130894263 | Common:3; Rare:105 | ||||
| chr3:131026720-131026968 | Common:2; Rare:64 | ||||
| chr3:131381425-131381843 | Common:3; Rare:116 | ||||
| chr3:131502809-131502995 | Common:1; Rare:89 | ||||
| chr3:132417177-132417757 | Common:6; Rare:188 | ||||
| chr3:132597014-132597290 | Common:1; Rare:33 | ||||
| chr3:132659783-132659974 | Common:3; Rare:45 | ||||
| chr3:132675058-132675383 | Rare:70; Clinvar (pathogenic):2 | ||||
| chr3:132721969-132722264 | Common:2; Rare:109; Clinvar:18; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr3:133573338-133573690 | Common:4; Rare:85 | ||||
| chr3:133573815-133574047 | Rare:79 | ||||
| chr3:133661789-133662011 | Rare:52 | ||||
| chr3:133895487-133895562 | Rare:23 | ||||
| chr3:134373720-134373815 | Rare:33 |