| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:14402411-14402632 | Common:1; Rare:57 | ||||
| chr3:14651474-14651807 | Rare:97 | ||||
| chr3:14947402-14947554 | Common:2; Rare:77 | ||||
| chr3:15099122-15099282 | Rare:36 | ||||
| chr3:15206016-15206279 | Rare:97 | ||||
| chr3:15427471-15427623 | Common:1; Rare:57 | ||||
| chr3:15601512-15601804 | Common:4; Rare:123; Clinvar:1 | ||||
| chr3:15859800-15860114 | Common:4; Rare:97 | ||||
| chr3:16264878-16265233 | Common:2; Rare:114 | ||||
| chr3:17742596-17742952 | Common:4; Rare:124 | ||||
| chr3:19946989-19947438 | Common:6; Rare:166 | ||||
| chr3:20186139-20186370 | Common:3; Rare:67 | ||||
| chr3:23916911-23917351 | Rare:149 | ||||
| chr3:25783386-25783621 | Common:2; Rare:78; Clinvar (benign):3 | ||||
| chr3:25789887-25790118 | Common:4; Rare:82 |