| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:45995736-45995911 | Rare:38; Clinvar:1 | ||||
| chr3:46208298-46208603 | Common:3; Rare:45 | ||||
| chr3:46370720-46370946 | Common:3; Rare:47; Clinvar (pathogenic):1 | ||||
| chr3:46407023-46407317 | Rare:56 | ||||
| chr3:46693670-46693815 | Common:1; Rare:32 | ||||
| chr3:46882119-46882264 | Common:1; Rare:45 | ||||
| chr3:46979508-46979846 | Common:2; Rare:81; Clinvar:1 | ||||
| chr3:47163933-47164265 | Common:1; Rare:93 | ||||
| chr3:47380806-47381080 | Rare:89 | ||||
| chr3:47381426-47381724 | Rare:71 | ||||
| chr3:47475812-47476068 | Common:3; Rare:106 | ||||
| chr3:47513335-47513602 | Common:1; Rare:98 | ||||
| chr3:47513663-47513767 | Rare:36 | ||||
| chr3:47781682-47782061 | Common:1; Rare:146 | ||||
| chr3:47802888-47803208 | Common:1; Rare:93 |