| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:146250967-146251229 | Common:1; Rare:63 | ||||
| chr3:146544471-146544865 | Common:5; Rare:92 | ||||
| chr3:148991386-148991656 | Common:2; Rare:121; Clinvar (benign):1 | ||||
| chr3:149129545-149129687 | Common:1; Rare:55; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:149377615-149377814 | Common:1; Rare:49 | ||||
| chr3:149657841-149658156 | Common:1; Rare:67 | ||||
| chr3:149658488-149658650 | Common:1; Rare:40 | ||||
| chr3:149812990-149813291 | Common:2; Rare:100 | ||||
| chr3:149971153-149971347 | Common:3; Rare:90 | ||||
| chr3:150408228-150408309 | Rare:40 | ||||
| chr3:150408602-150408667 | Rare:20 | ||||
| chr3:150410957-150411011 | Rare:18 | ||||
| chr3:150603147-150603398 | Common:2; Rare:100 | ||||
| chr3:152267771-152267866 | Rare:17 | ||||
| chr3:152268178-152268395 | Common:1; Rare:29 |