| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:33096731-33096857 | Rare:39 | ||||
| chr3:33097057-33097326 | Common:3; Rare:85; Clinvar:3; Clinvar (benign):1 | ||||
| chr3:33097433-33097594 | Common:2; Rare:35 | ||||
| chr3:33113789-33114027 | Common:2; Rare:57; Clinvar:1 | ||||
| chr3:33114031-33114588 | Common:2; Rare:235; Clinvar:15; Clinvar (benign):8; Clinvar (pathogenic):3 | ||||
| chr3:33115325-33115553 | Common:1; Rare:33 | ||||
| chr3:33439391-33439629 | Common:5; Rare:58 | ||||
| chr3:33439643-33439771 | Rare:41 | ||||
| chr3:33439925-33440184 | Rare:89 | ||||
| chr3:33440299-33440488 | Common:1; Rare:57 | ||||
| chr3:33440756-33441341 | Common:2; Rare:120 | ||||
| chr3:33659049-33659140 | Common:3; Rare:17 | ||||
| chr3:33659644-33659739 | Rare:29 | ||||
| chr3:33717738-33717895 | Rare:47 | ||||
| chr3:33717945-33718002 | Rare:20 |