| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:9933542-9933863 | Common:2; Rare:130; Clinvar:2 | ||||
| chr3:9934028-9934065 | Rare:10 | ||||
| chr3:9986759-9987163 | Common:4; Rare:117 | ||||
| chr3:10026334-10026465 | Rare:37 | ||||
| chr3:10115518-10115712 | Common:4; Rare:70 | ||||
| chr3:11137129-11137240 | Rare:23 | ||||
| chr3:11154338-11154538 | Common:4; Rare:53 | ||||
| chr3:11225829-11226036 | Rare:35 | ||||
| chr3:12484321-12484517 | Common:4; Rare:66; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:12664087-12664442 | Common:2; Rare:95; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:14124703-14125184 | Common:4; Rare:143; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178559-14178881 | Common:2; Rare:169; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:14651486-14651801 | Rare:90 | ||||
| chr3:14947244-14947554 | Common:3; Rare:143 | ||||
| chr3:15427459-15427623 | Common:1; Rare:61 |