| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:141231641-141231888 | Common:2; Rare:87 | ||||
| chr3:141368260-141368540 | Rare:58 | ||||
| chr3:141876486-141876652 | Common:1; Rare:61 | ||||
| chr3:142225469-142225678 | Common:3; Rare:74 | ||||
| chr3:142447974-142448122 | Common:1; Rare:51 | ||||
| chr3:142578711-142578963 | Rare:90; Clinvar:1 | ||||
| chr3:142723934-142724050 | Rare:30 | ||||
| chr3:143001405-143001647 | Common:3; Rare:93 | ||||
| chr3:143971760-143971829 | Common:1; Rare:31 | ||||
| chr3:143971887-143972075 | Common:1; Rare:69 | ||||
| chr3:146160962-146161279 | Common:1; Rare:106; Clinvar:4; Clinvar (benign):2 | ||||
| chr3:146250971-146251364 | Common:2; Rare:97 | ||||
| chr3:146544490-146544792 | Common:3; Rare:73 | ||||
| chr3:149086476-149086677 | Rare:60 | ||||
| chr3:149129549-149129701 | Common:1; Rare:62; Clinvar:2; Clinvar (benign):1 |