| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:141368235-141368572 | Rare:142 | ||||
| chr3:141402255-141402415 | Common:2; Rare:78 | ||||
| chr3:141402580-141403170 | Common:7; Rare:245 | ||||
| chr3:141486859-141487089 | Common:1; Rare:78 | ||||
| chr3:141487400-141487820 | Common:1; Rare:159 | ||||
| chr3:141738015-141738371 | Common:4; Rare:266 | ||||
| chr3:141875980-141876286 | Rare:151 | ||||
| chr3:141876428-141876911 | Common:6; Rare:351 | ||||
| chr3:142225402-142225657 | Common:6; Rare:154 | ||||
| chr3:142447939-142448145 | Common:2; Rare:136 | ||||
| chr3:142578395-142579011 | Common:1; Rare:304; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:142596282-142596450 | Common:1; Rare:44 | ||||
| chr3:142723830-142724130 | Common:1; Rare:121 | ||||
| chr3:142888867-142889149 | Common:6; Rare:108 | ||||
| chr3:143001010-143001650 | Common:8; Rare:251 |