| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:45026060-45026337 | Common:3; Rare:49 | ||||
| chr3:45689180-45689459 | Common:1; Rare:93 | ||||
| chr3:45995809-45995868 | Rare:14; Clinvar:1 | ||||
| chr3:47380838-47381073 | Rare:67 | ||||
| chr3:47475812-47476068 | Common:3; Rare:106 | ||||
| chr3:48088797-48089063 | Rare:90 | ||||
| chr3:48440081-48440307 | Common:1; Rare:88 | ||||
| chr3:48504045-48504277 | Common:2; Rare:74 | ||||
| chr3:48847675-48847973 | Common:1; Rare:84 | ||||
| chr3:48918765-48918889 | Common:2; Rare:72 | ||||
| chr3:49007361-49007428 | Rare:35 | ||||
| chr3:49022009-49022151 | Rare:45; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr3:49132969-49133148 | Rare:39; Clinvar:2 | ||||
| chr3:49340020-49340132 | Common:2; Rare:48 | ||||
| chr3:49411833-49412287 | Common:2; Rare:162 |