| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:149129545-149129739 | Common:1; Rare:83; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:149377370-149377824 | Common:1; Rare:135 | ||||
| chr3:149657689-149657840 | Common:2; Rare:36 | ||||
| chr3:149657947-149658181 | Rare:49 | ||||
| chr3:149752262-149752566 | Common:2; Rare:121 | ||||
| chr3:149813087-149813350 | Common:1; Rare:89 | ||||
| chr3:149971132-149971347 | Common:3; Rare:103 | ||||
| chr3:150408090-150408361 | Common:2; Rare:101 | ||||
| chr3:150408580-150408660 | Rare:27 | ||||
| chr3:150603115-150603499 | Common:3; Rare:143 | ||||
| chr3:150703176-150703552 | Rare:89 | ||||
| chr3:150703900-150704025 | Rare:44 | ||||
| chr3:151085567-151085789 | Rare:92 | ||||
| chr3:151086423-151086646 | Common:5; Rare:59 | ||||
| chr3:151249074-151249193 | Rare:26 |