| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:48695404-48695671 | Common:2; Rare:49 | ||||
| chr3:48847663-48847962 | Common:1; Rare:81 | ||||
| chr3:48918724-48918964 | Common:2; Rare:132 | ||||
| chr3:48982788-48982977 | Rare:35 | ||||
| chr3:48983063-48983233 | Rare:33 | ||||
| chr3:48989709-48989911 | Rare:55 | ||||
| chr3:48990776-48990882 | Rare:30 | ||||
| chr3:49007177-49007541 | Common:2; Rare:133 | ||||
| chr3:49018552-49018630 | Rare:28 | ||||
| chr3:49021498-49021720 | Rare:55; Clinvar:1 | ||||
| chr3:49022009-49022154 | Rare:47; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr3:49022500-49022767 | Common:1; Rare:101; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:49024034-49024359 | Common:2; Rare:84 | ||||
| chr3:49025125-49025531 | Common:1; Rare:91 | ||||
| chr3:49093585-49093634 | Rare:26 |