| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:123388651-123389021 | Common:1; Rare:98 | ||||
| chr12:123436449-123436605 | Rare:31 | ||||
| chr12:123436622-123436696 | Rare:13 | ||||
| chr12:123458062-123458651 | Common:6; Rare:132 | ||||
| chr12:123458874-123459028 | Rare:28 | ||||
| chr12:123533447-123533571 | Rare:37 | ||||
| chr12:123533694-123533890 | Common:1; Rare:56 | ||||
| chr12:123533964-123534213 | Common:2; Rare:78 | ||||
| chr12:123583977-123584153 | Rare:23 | ||||
| chr12:123584257-123584631 | Common:6; Rare:124 | ||||
| chr12:123585154-123585168 | Rare:5 | ||||
| chr12:123601748-123601896 | Rare:26 | ||||
| chr12:123601938-123602215 | Common:4; Rare:90 | ||||
| chr12:123633545-123634028 | Common:3; Rare:194; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:123670994-123671215 | Common:4; Rare:56; Clinvar:1; Clinvar (benign):1 |