| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:149129459-149129744 | Common:3; Rare:125; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:149130094-149130134 | Rare:4 | ||||
| chr3:149657910-149658268 | Rare:83 | ||||
| chr3:149658446-149658684 | Common:1; Rare:51 | ||||
| chr3:149752400-149752648 | Common:3; Rare:84 | ||||
| chr3:149812482-149812666 | Rare:44 | ||||
| chr3:149812669-149812829 | Common:1; Rare:51 | ||||
| chr3:149812984-149813339 | Common:2; Rare:112 | ||||
| chr3:149813706-149813830 | Common:1; Rare:20 | ||||
| chr3:149971182-149971347 | Common:3; Rare:78 | ||||
| chr3:150408226-150408744 | Common:2; Rare:180 | ||||
| chr3:150408798-150409016 | Rare:65 | ||||
| chr3:150546014-150546134 | Common:1; Rare:37 | ||||
| chr3:150546225-150547106 | Common:5; Rare:264 | ||||
| chr3:150603088-150603423 | Common:2; Rare:130 |