| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:43999119-43999462 | Rare:101 | ||||
| chr3:45076396-45076572 | Common:2; Rare:29 | ||||
| chr3:45167620-45167794 | Common:1; Rare:30 | ||||
| chr3:45704703-45704862 | Rare:27 | ||||
| chr3:48039443-48039489 | Rare:10 | ||||
| chr3:51340318-51340432 | Rare:14 | ||||
| chr3:51393055-51393098 | Rare:12 | ||||
| chr3:51935203-51935433 | Common:1; Rare:76 | ||||
| chr3:52407181-52407432 | Rare:59; Clinvar:6; Clinvar (benign):9 | ||||
| chr3:52712398-52712649 | Common:2; Rare:38 | ||||
| chr3:53197135-53197326 | Common:1; Rare:56 | ||||
| chr3:53228289-53228529 | Common:2; Rare:66 | ||||
| chr3:53233154-53233409 | Common:2; Rare:91; Clinvar (pathogenic):1 | ||||
| chr3:53238965-53239123 | Rare:21 | ||||
| chr3:55888499-55888807 | Common:1; Rare:71 |