| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:14124678-14125184 | Common:4; Rare:149; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178519-14178870 | Common:3; Rare:179; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr3:14651468-14651817 | Rare:103 | ||||
| chr3:14947149-14947563 | Common:5; Rare:173 | ||||
| chr3:14948017-14948177 | Rare:78 | ||||
| chr3:14948333-14948637 | Common:2; Rare:84 | ||||
| chr3:15032497-15032794 | Rare:67 | ||||
| chr3:15065159-15065378 | Common:2; Rare:81 | ||||
| chr3:15099109-15099293 | Rare:46 | ||||
| chr3:15205966-15206396 | Common:1; Rare:154 | ||||
| chr3:15427471-15427623 | Common:1; Rare:57 | ||||
| chr3:15428068-15428181 | Rare:14 | ||||
| chr3:15601502-15601804 | Common:4; Rare:125; Clinvar:1 | ||||
| chr3:15859511-15859606 | Common:2; Rare:25 | ||||
| chr3:15859782-15860114 | Common:4; Rare:104 |