| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:141402732-141403047 | Common:2; Rare:80 | ||||
| chr3:141486867-141487183 | Common:3; Rare:116; Clinvar:1 | ||||
| chr3:141578978-141579126 | Rare:26 | ||||
| chr3:141875989-141876175 | Rare:48 | ||||
| chr3:141876713-141876888 | Common:1; Rare:79 | ||||
| chr3:142225455-142225687 | Common:3; Rare:80 | ||||
| chr3:142596280-142596432 | Common:1; Rare:39 | ||||
| chr3:143001436-143001664 | Common:3; Rare:89 | ||||
| chr3:143026443-143026722 | Common:1; Rare:49 | ||||
| chr3:143971694-143971857 | Common:2; Rare:76 | ||||
| chr3:146070860-146071119 | Common:1; Rare:61; Clinvar:1 | ||||
| chr3:146160828-146161064 | Common:2; Rare:90; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:146161066-146161415 | Common:3; Rare:93; Clinvar:4; Clinvar (benign):2 | ||||
| chr3:146251035-146251207 | Common:1; Rare:42 | ||||
| chr3:148730135-148730234 | Rare:18 |