| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:140941655-140941878 | Common:2; Rare:84 | ||||
| chr3:141231644-141231889 | Common:2; Rare:85 | ||||
| chr3:141738096-141738357 | Common:2; Rare:111 | ||||
| chr3:141876480-141876656 | Common:1; Rare:64 | ||||
| chr3:142447974-142448116 | Common:1; Rare:49 | ||||
| chr3:142578720-142578980 | Rare:91; Clinvar:1 | ||||
| chr3:143001450-143001631 | Common:2; Rare:65 | ||||
| chr3:146160983-146161320 | Common:2; Rare:110; Clinvar:5; Clinvar (benign):2 | ||||
| chr3:149086488-149086735 | Rare:70 | ||||
| chr3:149129545-149129687 | Common:1; Rare:55; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:149377515-149377850 | Common:1; Rare:89 | ||||
| chr3:149813067-149813279 | Common:1; Rare:72 | ||||
| chr3:150603168-150603404 | Common:2; Rare:97 | ||||
| chr3:152268847-152268949 | Rare:37 | ||||
| chr3:155854374-155854593 | Rare:55 |