| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:47079728-47080073 | Common:4; Rare:83 | ||||
| chr12:47080349-47080608 | Common:1; Rare:46 | ||||
| chr12:47705960-47706124 | Rare:70 | ||||
| chr12:47753666-47753964 | Common:1; Rare:48 | ||||
| chr12:47758127-47758270 | Common:1; Rare:24 | ||||
| chr12:47758660-47759081 | Common:2; Rare:77 | ||||
| chr12:47759135-47759453 | Common:6; Rare:54 | ||||
| chr12:47771079-47771379 | Common:4; Rare:33 | ||||
| chr12:47773035-47773244 | Rare:72 | ||||
| chr12:47819857-47820167 | Common:3; Rare:74 | ||||
| chr12:47820561-47820902 | Rare:48 | ||||
| chr12:47904984-47905151 | Common:1; Rare:51; Clinvar:1 | ||||
| chr12:48105815-48105938 | Rare:28 | ||||
| chr12:48105979-48106213 | Common:2; Rare:78 | ||||
| chr12:48119192-48119382 | Common:2; Rare:37; Clinvar:4; Clinvar (benign):2 |