| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:129439829-129440418 | Common:1; Rare:186; Clinvar:3; Clinvar (benign):1 | ||||
| chr3:129688364-129688453 | Rare:20 | ||||
| chr3:129688627-129688705 | Common:1; Rare:16 | ||||
| chr3:129893545-129893916 | Rare:142 | ||||
| chr3:130746771-130746935 | Common:3; Rare:52 | ||||
| chr3:130893894-130894248 | Common:3; Rare:104 | ||||
| chr3:131026553-131026909 | Common:2; Rare:79 | ||||
| chr3:131381459-131381811 | Common:3; Rare:89 | ||||
| chr3:131502728-131503023 | Common:1; Rare:118 | ||||
| chr3:132417169-132417662 | Common:6; Rare:169 | ||||
| chr3:132659372-132659503 | Rare:17 | ||||
| chr3:132659799-132659946 | Common:3; Rare:35 | ||||
| chr3:133038178-133038428 | Common:1; Rare:88 | ||||
| chr3:133661760-133662062 | Rare:70 | ||||
| chr3:134374425-134374679 | Common:1; Rare:76 |