| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:33277312-33277482 | Common:1; Rare:45 | ||||
| chr3:33440904-33441088 | Rare:39 | ||||
| chr3:33718061-33718308 | Rare:92 | ||||
| chr3:33798484-33798686 | Common:2; Rare:72 | ||||
| chr3:33798985-33799167 | Rare:58 | ||||
| chr3:36944846-36945199 | Common:1; Rare:83 | ||||
| chr3:36993056-36993586 | Common:2; Rare:187; Clinvar:34; Clinvar (benign):15; Clinvar (pathogenic):4 | ||||
| chr3:37176237-37176393 | Rare:51 | ||||
| chr3:37243166-37243429 | Common:1; Rare:62 | ||||
| chr3:37243443-37243583 | Rare:46 | ||||
| chr3:37994086-37994208 | Rare:34 | ||||
| chr3:38024501-38024680 | Common:1; Rare:68 | ||||
| chr3:38029612-38029844 | Common:1; Rare:46 | ||||
| chr3:38138549-38138811 | Common:2; Rare:96; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:38165446-38165514 | Rare:19 |