| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:129183814-129184079 | Common:2; Rare:89 | ||||
| chr3:129316283-129316360 | Common:1; Rare:25 | ||||
| chr3:129440007-129440313 | Common:1; Rare:83; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:129893580-129893882 | Rare:129 | ||||
| chr3:130746796-130746971 | Common:3; Rare:48 | ||||
| chr3:134485701-134485766 | Rare:26 | ||||
| chr3:134485977-134486233 | Common:3; Rare:82 | ||||
| chr3:136862000-136862284 | Common:1; Rare:90 | ||||
| chr3:139389578-139389842 | Common:1; Rare:87 | ||||
| chr3:143001472-143001631 | Common:2; Rare:57 | ||||
| chr3:146161077-146161386 | Common:2; Rare:83; Clinvar:3; Clinvar (benign):1 | ||||
| chr3:149813067-149813260 | Common:1; Rare:65 | ||||
| chr3:150603176-150603404 | Common:2; Rare:95 | ||||
| chr3:152268805-152268961 | Rare:60 | ||||
| chr3:155870329-155870744 | Common:2; Rare:116 |