| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:37176140-37176371 | Rare:61 | ||||
| chr3:37242967-37243474 | Common:5; Rare:131 | ||||
| chr3:38024475-38024598 | Common:1; Rare:47 | ||||
| chr3:38029585-38029929 | Common:2; Rare:66 | ||||
| chr3:38138374-38138703 | Common:2; Rare:97; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr3:38165450-38165817 | Common:1; Rare:124 | ||||
| chr3:39051973-39052046 | Common:1; Rare:27 | ||||
| chr3:39107555-39107812 | Common:5; Rare:76 | ||||
| chr3:39153524-39153767 | Common:3; Rare:85 | ||||
| chr3:39383319-39383432 | Common:1; Rare:23; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:39383524-39383676 | Rare:32; Clinvar:2 | ||||
| chr3:39406574-39406761 | Common:2; Rare:79 | ||||
| chr3:40309459-40309807 | Common:9; Rare:116 | ||||
| chr3:40505945-40506132 | Rare:40 | ||||
| chr3:40524815-40525006 | Common:1; Rare:55 |