| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:129794507-129794687 | Rare:32 | ||||
| chr3:129847330-129847676 | Rare:72 | ||||
| chr3:129847930-129848303 | Rare:89 | ||||
| chr3:130111422-130111675 | Common:3; Rare:72 | ||||
| chr3:130958021-130958218 | Common:1; Rare:32 | ||||
| chr3:130960411-130960918 | Common:3; Rare:76 | ||||
| chr3:130968193-130968497 | Common:3; Rare:54 | ||||
| chr3:130975428-130975551 | Rare:38; Clinvar (benign):1 | ||||
| chr3:130979184-130979314 | Rare:36; Clinvar (benign):1 | ||||
| chr3:130990886-130991161 | Common:1; Rare:49 | ||||
| chr3:130991566-130991839 | Common:2; Rare:44 | ||||
| chr3:131361705-131361931 | Common:2; Rare:66 | ||||
| chr3:132663295-132663532 | Rare:34 | ||||
| chr3:132668589-132668910 | Common:3; Rare:61 | ||||
| chr3:132718641-132718701 | Rare:12 |