| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:141876441-141876772 | Common:3; Rare:135 | ||||
| chr3:142578700-142578925 | Rare:79; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:142888978-142889304 | Common:3; Rare:59 | ||||
| chr3:143001436-143001638 | Common:3; Rare:74 | ||||
| chr3:143971938-143972102 | Common:1; Rare:63 | ||||
| chr3:146544458-146544792 | Common:4; Rare:80 | ||||
| chr3:148991383-148991632 | Common:2; Rare:115; Clinvar (benign):1 | ||||
| chr3:149129545-149129687 | Common:1; Rare:55; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:149377482-149377844 | Common:1; Rare:99 | ||||
| chr3:149657948-149658086 | Rare:23 | ||||
| chr3:149812626-149812786 | Common:1; Rare:45 | ||||
| chr3:149813120-149813291 | Common:1; Rare:61 | ||||
| chr3:149970855-149971055 | Common:1; Rare:98 | ||||
| chr3:150407987-150408320 | Common:2; Rare:98 | ||||
| chr3:150603145-150603404 | Common:2; Rare:103 |