| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:33097103-33097215 | Rare:36; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:33277289-33277482 | Common:2; Rare:52 | ||||
| chr3:33440946-33441060 | Rare:17 | ||||
| chr3:33798477-33798686 | Common:2; Rare:76 | ||||
| chr3:33798990-33799157 | Rare:54 | ||||
| chr3:36993161-36993559 | Common:2; Rare:119; Clinvar:26; Clinvar (benign):12; Clinvar (pathogenic):3 | ||||
| chr3:37243166-37243310 | Common:1; Rare:34 | ||||
| chr3:38138576-38138698 | Common:2; Rare:49; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr3:39153550-39153758 | Common:3; Rare:69 | ||||
| chr3:39383306-39383422 | Rare:23; Clinvar:1 | ||||
| chr3:39383582-39383676 | Rare:20; Clinvar:1 | ||||
| chr3:40309479-40309816 | Common:9; Rare:115 | ||||
| chr3:40505853-40506137 | Rare:70 | ||||
| chr3:40524815-40524911 | Common:1; Rare:26 | ||||
| chr3:42581900-42582132 | Common:3; Rare:70 |