| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:48105846-48105941 | Rare:23 | ||||
| chr12:48105977-48106206 | Common:2; Rare:74 | ||||
| chr12:48106277-48106419 | Rare:43 | ||||
| chr12:48184023-48184118 | Common:3; Rare:31 | ||||
| chr12:48350771-48350956 | Rare:68 | ||||
| chr12:48351248-48351325 | Common:1; Rare:12 | ||||
| chr12:48716644-48717111 | Common:5; Rare:146 | ||||
| chr12:48814166-48814507 | Common:5; Rare:61 | ||||
| chr12:48814684-48814862 | Rare:31 | ||||
| chr12:48815432-48815613 | Common:1; Rare:41 | ||||
| chr12:48852102-48852413 | Common:2; Rare:84 | ||||
| chr12:49018741-49018927 | Common:1; Rare:74 | ||||
| chr12:49131298-49131619 | Common:2; Rare:126 | ||||
| chr12:49186773-49186987 | Common:1; Rare:31; Clinvar:1; Clinvar (benign):2 | ||||
| chr12:49188488-49188607 | Common:2; Rare:17 |