| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:48814664-48814872 | Rare:36 | ||||
| chr12:48815261-48815608 | Common:1; Rare:81 | ||||
| chr12:48852086-48852385 | Common:2; Rare:86 | ||||
| chr12:48865864-48866013 | Rare:36 | ||||
| chr12:48957287-48957578 | Common:2; Rare:83 | ||||
| chr12:49018736-49018926 | Rare:78 | ||||
| chr12:49131296-49131606 | Common:2; Rare:124 | ||||
| chr12:49188981-49189281 | Rare:82; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:49264775-49265096 | Common:4; Rare:116 | ||||
| chr12:49568086-49568192 | Common:2; Rare:39 | ||||
| chr12:49707056-49707098 | Rare:10 | ||||
| chr12:50085067-50085372 | Common:1; Rare:81 | ||||
| chr12:50167304-50167656 | Common:2; Rare:99 | ||||
| chr12:50283481-50283654 | Common:1; Rare:56 | ||||
| chr12:50400712-50400968 | Rare:77 |