| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:139539554-139539693 | Common:3; Rare:49 | ||||
| chr3:139539695-139539782 | Rare:23 | ||||
| chr3:140941655-140941931 | Common:2; Rare:102 | ||||
| chr3:141231641-141231888 | Common:2; Rare:87 | ||||
| chr3:141386135-141386473 | Common:1; Rare:55 | ||||
| chr3:141386749-141387018 | Common:1; Rare:42 | ||||
| chr3:141486794-141487086 | Common:1; Rare:89 | ||||
| chr3:141876060-141876179 | Rare:32 | ||||
| chr3:142447974-142448098 | Rare:45 | ||||
| chr3:142578700-142578998 | Rare:113; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:142723901-142724040 | Rare:42 | ||||
| chr3:143001444-143001631 | Common:3; Rare:67 | ||||
| chr3:146544623-146544952 | Common:1; Rare:86 | ||||
| chr3:147409155-147409418 | Rare:83 | ||||
| chr3:149086471-149086711 | Rare:71 |