| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:69084762-69085102 | Common:3; Rare:87 | ||||
| chr3:69200480-69200679 | Common:1; Rare:29 | ||||
| chr3:71130539-71130694 | Common:1; Rare:62; Clinvar:2 | ||||
| chr3:71582162-71582396 | Rare:75 | ||||
| chr3:71754767-71755060 | Rare:94 | ||||
| chr3:72996720-72997030 | Common:1; Rare:116 | ||||
| chr3:81761637-81761705 | Rare:22 | ||||
| chr3:88058946-88059322 | Common:2; Rare:143 | ||||
| chr3:88149613-88149682 | Common:1; Rare:17 | ||||
| chr3:88149864-88150043 | Common:5; Rare:74 | ||||
| chr3:93973771-93974028 | Rare:76; Clinvar:6 | ||||
| chr3:93979970-93980195 | Common:4; Rare:79; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:94062977-94063091 | Rare:21 | ||||
| chr3:97764496-97764541 | Rare:6 | ||||
| chr3:97764706-97764795 | Common:1; Rare:17; Clinvar (benign):1 |