| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:141876472-141876680 | Common:1; Rare:80 | ||||
| chr3:142447945-142448137 | Common:1; Rare:67 | ||||
| chr3:142578721-142578764 | Rare:22 | ||||
| chr3:142596300-142596414 | Common:1; Rare:30 | ||||
| chr3:143001454-143001634 | Common:2; Rare:63 | ||||
| chr3:143971702-143971852 | Common:2; Rare:69 | ||||
| chr3:146544514-146544858 | Common:4; Rare:81 | ||||
| chr3:149086494-149086699 | Rare:58 | ||||
| chr3:149129596-149129726 | Common:1; Rare:58; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:149377640-149377874 | Common:1; Rare:53 | ||||
| chr3:149813107-149813273 | Common:1; Rare:62 | ||||
| chr3:150408078-150408367 | Common:2; Rare:105 | ||||
| chr3:150603147-150603305 | Common:1; Rare:49 | ||||
| chr3:150703400-150703543 | Rare:40 | ||||
| chr3:151086749-151086914 | Common:1; Rare:51 |