| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:48301325-48301651 | Common:4; Rare:104 | ||||
| chr3:48440007-48440434 | Common:3; Rare:177 | ||||
| chr3:48446619-48446743 | Rare:45 | ||||
| chr3:48473031-48473265 | Common:2; Rare:54 | ||||
| chr3:48556784-48557229 | Common:1; Rare:112 | ||||
| chr3:48635407-48635627 | Rare:73 | ||||
| chr3:48847682-48847973 | Common:1; Rare:83 | ||||
| chr3:48898837-48899081 | Rare:69; Clinvar:6 | ||||
| chr3:48918696-48918912 | Common:2; Rare:107 | ||||
| chr3:49007155-49007426 | Common:2; Rare:111 | ||||
| chr3:49021500-49021646 | Rare:40 | ||||
| chr3:49029368-49029564 | Common:2; Rare:140 | ||||
| chr3:49094023-49094131 | Rare:23 | ||||
| chr3:49104439-49104551 | Rare:43; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr3:49104615-49104910 | Common:1; Rare:120; Clinvar:3; Clinvar (benign):7 |