| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:48847663-48847966 | Common:1; Rare:83 | ||||
| chr3:48918787-48918930 | Common:2; Rare:86 | ||||
| chr3:49007124-49007434 | Common:2; Rare:124 | ||||
| chr3:49018552-49018611 | Rare:22 | ||||
| chr3:49021502-49021703 | Rare:51; Clinvar:1 | ||||
| chr3:49028275-49028490 | Rare:67 | ||||
| chr3:49100080-49100232 | Rare:50; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr3:49104391-49104567 | Rare:61; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr3:49104615-49104897 | Common:1; Rare:114; Clinvar:3; Clinvar (benign):7 | ||||
| chr3:49132969-49133148 | Rare:39; Clinvar:2 | ||||
| chr3:49166271-49166437 | Common:1; Rare:44 | ||||
| chr3:49171450-49171646 | Common:2; Rare:40 | ||||
| chr3:49339984-49340162 | Common:2; Rare:76 | ||||
| chr3:49358025-49358458 | Common:4; Rare:221 | ||||
| chr3:49411821-49412375 | Common:2; Rare:189 |