| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:23805834-23806061 | Common:1; Rare:47 | ||||
| chr3:23866001-23866412 | Common:1; Rare:76 | ||||
| chr3:23916839-23917214 | Rare:140 | ||||
| chr3:25783377-25783621 | Common:2; Rare:83; Clinvar (benign):3 | ||||
| chr3:25790008-25790126 | Common:4; Rare:45 | ||||
| chr3:27484078-27484219 | Common:2; Rare:48 | ||||
| chr3:28241555-28241783 | Common:2; Rare:80 | ||||
| chr3:28348583-28349203 | Common:4; Rare:183 | ||||
| chr3:29280831-29281393 | Common:15; Rare:110 | ||||
| chr3:30606394-30606513 | Rare:26 | ||||
| chr3:31532070-31532180 | Common:2; Rare:31 | ||||
| chr3:31532355-31532638 | Common:2; Rare:83 | ||||
| chr3:31532939-31533301 | Common:2; Rare:128; Clinvar (benign):2 | ||||
| chr3:31981603-31981810 | Common:1; Rare:54 | ||||
| chr3:32106378-32106703 | Common:4; Rare:91; Clinvar:2; Clinvar (benign):1 |