| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:141431430-141431800 | Rare:101 | ||||
| chr3:141431972-141432225 | Common:2; Rare:36 | ||||
| chr3:141738027-141738374 | Common:4; Rare:279 | ||||
| chr3:141876491-141876778 | Common:3; Rare:120 | ||||
| chr3:142225404-142225673 | Common:4; Rare:130 | ||||
| chr3:142447954-142448153 | Common:2; Rare:142 | ||||
| chr3:142578698-142578954 | Rare:168; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:142596272-142596451 | Common:2; Rare:94 | ||||
| chr3:142723908-142724129 | Common:1; Rare:106 | ||||
| chr3:142724316-142724590 | Common:6; Rare:137 | ||||
| chr3:142724960-142725078 | Rare:34 | ||||
| chr3:142963589-142963982 | Common:10; Rare:205 | ||||
| chr3:143001423-143001638 | Common:6; Rare:153 | ||||
| chr3:143971593-143971845 | Common:2; Rare:165 | ||||
| chr3:143972800-143973250 | Common:3; Rare:156 |