| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:129249549-129249683 | Common:1; Rare:43 | ||||
| chr3:129316261-129316350 | Rare:35 | ||||
| chr3:129439847-129440254 | Common:1; Rare:120; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:129893501-129893887 | Rare:143 | ||||
| chr3:130893938-130894240 | Common:3; Rare:91 | ||||
| chr3:131026749-131026909 | Common:2; Rare:41 | ||||
| chr3:131381479-131381850 | Common:2; Rare:106 | ||||
| chr3:131502814-131503023 | Common:1; Rare:90 | ||||
| chr3:132417213-132417549 | Common:2; Rare:103 | ||||
| chr3:132659806-132659950 | Common:3; Rare:34 | ||||
| chr3:134485442-134485877 | Common:1; Rare:111 | ||||
| chr3:134485947-134486453 | Common:7; Rare:169 | ||||
| chr3:136862000-136862303 | Common:1; Rare:97 | ||||
| chr3:139359350-139359497 | Rare:34 | ||||
| chr3:139389576-139389868 | Common:1; Rare:93 |