| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:142225491-142225631 | Common:3; Rare:50 | ||||
| chr3:142225634-142225653 | Rare:3 | ||||
| chr3:142447968-142448122 | Common:1; Rare:55 | ||||
| chr3:142578700-142578962 | Rare:98; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:142596243-142596418 | Common:2; Rare:45 | ||||
| chr3:142723895-142724074 | Rare:53 | ||||
| chr3:142888889-142889018 | Common:3; Rare:38 | ||||
| chr3:143001405-143001654 | Common:3; Rare:97 | ||||
| chr3:143971717-143971837 | Common:1; Rare:53 | ||||
| chr3:143971961-143972074 | Rare:43 | ||||
| chr3:147393351-147393744 | Common:1; Rare:114 | ||||
| chr3:147397168-147397505 | Common:3; Rare:67 | ||||
| chr3:147409155-147409496 | Rare:97 | ||||
| chr3:149086445-149086711 | Rare:80 | ||||
| chr3:149129545-149129721 | Common:1; Rare:73; Clinvar:2; Clinvar (benign):1 |