| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:129439847-129440350 | Common:1; Rare:155; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:129893523-129893882 | Rare:137 | ||||
| chr3:130746796-130746934 | Common:3; Rare:40 | ||||
| chr3:130893919-130894227 | Common:3; Rare:91 | ||||
| chr3:131026720-131026947 | Common:2; Rare:56 | ||||
| chr3:131381462-131381801 | Common:3; Rare:85 | ||||
| chr3:131502814-131503013 | Common:1; Rare:89 | ||||
| chr3:132417212-132417534 | Common:2; Rare:97 | ||||
| chr3:132659799-132659950 | Common:3; Rare:35 | ||||
| chr3:132722018-132722230 | Common:1; Rare:88; Clinvar:15; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr3:133573753-133573966 | Rare:63 | ||||
| chr3:133661844-133662010 | Rare:39 | ||||
| chr3:134374411-134374691 | Common:1; Rare:84 | ||||
| chr3:134485694-134485766 | Rare:29 | ||||
| chr3:134485957-134486229 | Common:2; Rare:93 |