| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:25790008-25790118 | Common:3; Rare:42 | ||||
| chr3:28348779-28349191 | Common:4; Rare:129 | ||||
| chr3:29280829-29280911 | Common:1; Rare:17 | ||||
| chr3:29280975-29281082 | Common:1; Rare:18 | ||||
| chr3:31532380-31532643 | Common:2; Rare:71 | ||||
| chr3:32106431-32106714 | Common:3; Rare:74; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:32570747-32570966 | Common:1; Rare:94 | ||||
| chr3:33277325-33277489 | Common:1; Rare:42 | ||||
| chr3:33798520-33798681 | Common:2; Rare:57 | ||||
| chr3:35639722-35639877 | Common:1; Rare:36 | ||||
| chr3:36993073-36993550 | Common:2; Rare:160; Clinvar:26; Clinvar (benign):10; Clinvar (pathogenic):2 | ||||
| chr3:37176131-37176387 | Rare:71 | ||||
| chr3:38024510-38024652 | Common:1; Rare:52 | ||||
| chr3:39051944-39052042 | Common:1; Rare:35 | ||||
| chr3:39107574-39107680 | Common:2; Rare:34 |