| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:4493177-4493483 | Rare:110; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:4979154-4979576 | Common:2; Rare:99 | ||||
| chr3:4979580-4979668 | Common:1; Rare:18 | ||||
| chr3:4980361-4980576 | Common:1; Rare:56 | ||||
| chr3:5187460-5187663 | Common:3; Rare:87 | ||||
| chr3:8501621-8501668 | Rare:20 | ||||
| chr3:8501676-8501935 | Common:2; Rare:93 | ||||
| chr3:9249551-9249816 | Common:2; Rare:54 | ||||
| chr3:9362959-9363096 | Common:2; Rare:51 | ||||
| chr3:9397436-9397685 | Rare:90 | ||||
| chr3:9749790-9750018 | Common:1; Rare:76 | ||||
| chr3:9769881-9770037 | Common:1; Rare:42 | ||||
| chr3:9792363-9792499 | Rare:40 | ||||
| chr3:9792732-9793118 | Common:3; Rare:132 | ||||
| chr3:9916912-9917167 | Common:3; Rare:58 |