| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:47758819-47759011 | Common:1; Rare:38 | ||||
| chr12:48105997-48106116 | Common:1; Rare:33 | ||||
| chr12:48106121-48106208 | Common:1; Rare:35 | ||||
| chr12:48350790-48350963 | Rare:63 | ||||
| chr12:48716676-48717008 | Common:4; Rare:100 | ||||
| chr12:48818583-48818828 | Common:1; Rare:86 | ||||
| chr12:48852119-48852378 | Common:2; Rare:71 | ||||
| chr12:48865845-48866039 | Common:1; Rare:47 | ||||
| chr12:48957367-48957581 | Common:2; Rare:58 | ||||
| chr12:49018739-49018935 | Common:1; Rare:81 | ||||
| chr12:49131302-49131679 | Common:2; Rare:149 | ||||
| chr12:49188455-49188607 | Common:2; Rare:22 | ||||
| chr12:49188975-49189288 | Rare:84; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:49264781-49265082 | Common:4; Rare:104 | ||||
| chr12:49296961-49297259 | Common:1; Rare:104; Clinvar:2 |