| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:69542567-69542845 | Common:2; Rare:80 | ||||
| chr3:69739216-69739492 | Rare:90 | ||||
| chr3:69866123-69866284 | Rare:30 | ||||
| chr3:71130558-71130677 | Rare:47; Clinvar:1 | ||||
| chr3:72996709-72997044 | Common:2; Rare:125 | ||||
| chr3:75785505-75785669 | Common:2; Rare:19 | ||||
| chr3:81761515-81761834 | Common:8; Rare:106; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:87227202-87227401 | Common:1; Rare:68; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:88058923-88059313 | Common:3; Rare:146 | ||||
| chr3:88149605-88149757 | Common:1; Rare:34 | ||||
| chr3:88149856-88150055 | Common:5; Rare:79 | ||||
| chr3:93973800-93973959 | Rare:47; Clinvar:4 | ||||
| chr3:93979935-93980232 | Common:4; Rare:114; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:94062763-94063134 | Common:4; Rare:92 | ||||
| chr3:96814453-96814586 | Rare:53 |