| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:122564252-122564419 | Common:2; Rare:50 | ||||
| chr3:123066888-123067177 | Rare:72 | ||||
| chr3:123585032-123585317 | Common:1; Rare:86 | ||||
| chr3:123585491-123585590 | Rare:19 | ||||
| chr3:125375237-125375431 | Rare:60 | ||||
| chr3:125520153-125520345 | Rare:56 | ||||
| chr3:127598269-127598458 | Common:2; Rare:53 | ||||
| chr3:127822451-127822557 | Rare:23 | ||||
| chr3:128052170-128052515 | Common:2; Rare:117 | ||||
| chr3:128153350-128153493 | Rare:37 | ||||
| chr3:128487920-128488107 | Rare:50 | ||||
| chr3:128879408-128879669 | Common:4; Rare:126; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:129183814-129184079 | Common:2; Rare:89 | ||||
| chr3:129249503-129249688 | Common:3; Rare:53 | ||||
| chr3:129439832-129440381 | Common:1; Rare:166; Clinvar:2; Clinvar (benign):1 |