| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:142225538-142225661 | Common:1; Rare:37 | ||||
| chr3:142447975-142448122 | Common:1; Rare:50 | ||||
| chr3:142578711-142578925 | Rare:71; Clinvar:1 | ||||
| chr3:142596116-142596424 | Common:3; Rare:77 | ||||
| chr3:142723901-142724037 | Rare:41 | ||||
| chr3:143001472-143001661 | Common:2; Rare:72 | ||||
| chr3:143971760-143971837 | Common:1; Rare:36 | ||||
| chr3:143971853-143972074 | Rare:74 | ||||
| chr3:146160961-146161320 | Common:2; Rare:117; Clinvar:5; Clinvar (benign):2 | ||||
| chr3:146544540-146544847 | Common:4; Rare:71 | ||||
| chr3:147409219-147409422 | Rare:76 | ||||
| chr3:149086452-149086722 | Rare:80 | ||||
| chr3:149129545-149129687 | Common:1; Rare:55; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:149377628-149377835 | Common:1; Rare:48 | ||||
| chr3:149752386-149752566 | Common:2; Rare:68 |