| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:36993117-36993553 | Common:2; Rare:135; Clinvar:26; Clinvar (benign):10; Clinvar (pathogenic):3 | ||||
| chr3:37242921-37243361 | Common:6; Rare:117 | ||||
| chr3:39051944-39052035 | Common:1; Rare:34 | ||||
| chr3:39107597-39107716 | Common:3; Rare:36 | ||||
| chr3:39383324-39383660 | Common:3; Rare:77; Clinvar:7; Clinvar (benign):2 | ||||
| chr3:39406932-39407067 | Common:1; Rare:56 | ||||
| chr3:40309477-40309872 | Common:9; Rare:132 | ||||
| chr3:40524812-40524911 | Common:1; Rare:26 | ||||
| chr3:42581904-42582109 | Common:2; Rare:66 | ||||
| chr3:42804440-42804649 | Common:2; Rare:61 | ||||
| chr3:42936331-42936438 | Common:1; Rare:31 | ||||
| chr3:44477655-44477707 | Common:1; Rare:10 | ||||
| chr3:44510591-44510782 | Common:2; Rare:48 | ||||
| chr3:44624905-44625056 | Common:1; Rare:40 | ||||
| chr3:44729552-44729667 | Common:1; Rare:44 |