| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:36993056-36993559 | Common:2; Rare:172; Clinvar:26; Clinvar (benign):12; Clinvar (pathogenic):3 | ||||
| chr3:37176021-37176393 | Common:1; Rare:104 | ||||
| chr3:37243166-37243483 | Common:1; Rare:78 | ||||
| chr3:38024470-38024664 | Common:1; Rare:74 | ||||
| chr3:38029600-38029879 | Common:1; Rare:56 | ||||
| chr3:38138521-38138707 | Common:2; Rare:68; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr3:38165437-38165817 | Common:1; Rare:125 | ||||
| chr3:39051944-39052057 | Common:1; Rare:42 | ||||
| chr3:39107555-39107680 | Common:2; Rare:40 | ||||
| chr3:39153461-39153737 | Common:3; Rare:90 | ||||
| chr3:39383286-39383448 | Common:2; Rare:31; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:39383554-39383700 | Rare:35; Clinvar:2 | ||||
| chr3:40309456-40309935 | Common:9; Rare:159 | ||||
| chr3:40387047-40387249 | Common:2; Rare:62 | ||||
| chr3:40457221-40457403 | Common:3; Rare:92 |