| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:25719497-25719861 | Rare:91; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr3:25746610-25746687 | Rare:10 | ||||
| chr3:25749263-25749717 | Common:1; Rare:89 | ||||
| chr3:25749732-25749885 | Common:3; Rare:23 | ||||
| chr3:27409000-27409131 | Rare:26 | ||||
| chr3:27432487-27432639 | Rare:27 | ||||
| chr3:27433682-27433961 | Common:4; Rare:65 | ||||
| chr3:27458550-27458780 | Common:1; Rare:48 | ||||
| chr3:27465177-27465466 | Common:6; Rare:40 | ||||
| chr3:27481752-27482089 | Common:2; Rare:77 | ||||
| chr3:27497608-27497683 | Rare:13 | ||||
| chr3:27624172-27624224 | Common:1; Rare:6 | ||||
| chr3:28113120-28113162 | Rare:10 | ||||
| chr3:28308839-28309061 | Common:11; Rare:60 | ||||
| chr3:29282437-29282764 | Common:1; Rare:59 |