| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:14178559-14178870 | Common:2; Rare:163; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:14402479-14402610 | Rare:37 | ||||
| chr3:14651486-14651847 | Rare:114 | ||||
| chr3:14947209-14947583 | Common:4; Rare:165 | ||||
| chr3:15206047-15206248 | Rare:68 | ||||
| chr3:15427460-15427623 | Common:1; Rare:61 | ||||
| chr3:15601504-15601801 | Common:4; Rare:124; Clinvar:1 | ||||
| chr3:15859782-15860130 | Common:4; Rare:112 | ||||
| chr3:16264882-16265237 | Common:2; Rare:117 | ||||
| chr3:16513629-16513841 | Common:4; Rare:50 | ||||
| chr3:19947013-19947450 | Common:6; Rare:164 | ||||
| chr3:23916911-23917208 | Rare:114 | ||||
| chr3:23917648-23918003 | Common:2; Rare:92; Clinvar (benign):1 | ||||
| chr3:25783387-25783621 | Common:2; Rare:78; Clinvar (benign):3 | ||||
| chr3:25789936-25790126 | Common:5; Rare:72 |