| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:48473042-48473242 | Common:1; Rare:44 | ||||
| chr3:48556752-48557173 | Common:1; Rare:103 | ||||
| chr3:48635435-48635627 | Rare:60 | ||||
| chr3:48685838-48685996 | Common:1; Rare:56 | ||||
| chr3:48847639-48847966 | Common:1; Rare:89 | ||||
| chr3:48918734-48918922 | Common:2; Rare:103 | ||||
| chr3:49007326-49007434 | Common:1; Rare:55 | ||||
| chr3:49021503-49021713 | Rare:53; Clinvar:1 | ||||
| chr3:49022082-49022174 | Rare:39; Clinvar (pathogenic):1 | ||||
| chr3:49029320-49029475 | Common:1; Rare:103 | ||||
| chr3:49104703-49104910 | Common:1; Rare:88; Clinvar:1; Clinvar (benign):5 | ||||
| chr3:49132944-49133082 | Rare:24; Clinvar:1 | ||||
| chr3:49199159-49199547 | Common:1; Rare:84 | ||||
| chr3:49277048-49277112 | Rare:21 | ||||
| chr3:49340020-49340221 | Common:2; Rare:73 |