| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:23916866-23917208 | Rare:134 | ||||
| chr3:25783392-25783627 | Common:2; Rare:76; Clinvar (benign):3 | ||||
| chr3:27194176-27194291 | Common:1; Rare:27 | ||||
| chr3:28349041-28349170 | Common:2; Rare:39 | ||||
| chr3:29280843-29281081 | Common:3; Rare:45 | ||||
| chr3:32570756-32570956 | Common:1; Rare:90 | ||||
| chr3:33218800-33218974 | Common:3; Rare:50 | ||||
| chr3:33277306-33277501 | Common:1; Rare:54 | ||||
| chr3:33718086-33718291 | Rare:76 | ||||
| chr3:33798514-33798676 | Common:2; Rare:57 | ||||
| chr3:36993078-36993564 | Common:2; Rare:166; Clinvar:27; Clinvar (benign):12; Clinvar (pathogenic):3 | ||||
| chr3:36993690-36993830 | Rare:57; Clinvar:1 | ||||
| chr3:37243166-37243381 | Common:1; Rare:54 | ||||
| chr3:39051944-39052042 | Common:1; Rare:35 | ||||
| chr3:39107574-39107658 | Common:1; Rare:32 |