| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:44861980-44862350 | Common:4; Rare:113 | ||||
| chr3:44975951-44976295 | Common:7; Rare:206 | ||||
| chr3:45388386-45388680 | Common:4; Rare:145 | ||||
| chr3:45593752-45594243 | Common:10; Rare:230 | ||||
| chr3:45689147-45689465 | Common:3; Rare:204 | ||||
| chr3:45842070-45842295 | Common:2; Rare:109 | ||||
| chr3:45995719-45995914 | Common:1; Rare:72; Clinvar:2 | ||||
| chr3:46163139-46163487 | Rare:54 | ||||
| chr3:46163653-46163793 | Rare:24 | ||||
| chr3:46407051-46407268 | Rare:76 | ||||
| chr3:46693547-46693787 | Common:3; Rare:88 | ||||
| chr3:46976578-46977200 | Common:7; Rare:211 | ||||
| chr3:46979494-46979880 | Common:5; Rare:188; Clinvar:3 | ||||
| chr3:47163185-47163381 | Common:1; Rare:41 | ||||
| chr3:47163883-47164503 | Common:3; Rare:221; Clinvar (pathogenic):1 |