| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:69542581-69542769 | Common:2; Rare:53 | ||||
| chr3:71130558-71130674 | Rare:45; Clinvar:1 | ||||
| chr3:72996709-72997030 | Common:2; Rare:120 | ||||
| chr3:75785538-75785680 | Common:2; Rare:12 | ||||
| chr3:79767537-79767789 | Common:4; Rare:40 | ||||
| chr3:79767940-79768068 | Rare:21 | ||||
| chr3:81761510-81761698 | Common:7; Rare:65; Clinvar (benign):1 | ||||
| chr3:84958776-84959033 | Common:4; Rare:89 | ||||
| chr3:87227186-87227409 | Common:1; Rare:75; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:88058932-88059322 | Common:3; Rare:148 | ||||
| chr3:88149812-88150033 | Common:2; Rare:68 | ||||
| chr3:94062897-94063040 | Rare:41 | ||||
| chr3:97764458-97764795 | Common:1; Rare:78; Clinvar (benign):1 | ||||
| chr3:97821866-97822107 | Rare:87 | ||||
| chr3:98522847-98523135 | Common:1; Rare:85 |