| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:89524551-89524594 | Rare:17 | ||||
| chr12:89524748-89524869 | Common:1; Rare:22 | ||||
| chr12:89525889-89526020 | Common:1; Rare:55 | ||||
| chr12:89708820-89709097 | Common:1; Rare:106 | ||||
| chr12:92929126-92929495 | Common:2; Rare:110 | ||||
| chr12:93377728-93377929 | Rare:54 | ||||
| chr12:93441883-93442178 | Common:2; Rare:96 | ||||
| chr12:93571755-93571912 | Common:7; Rare:61 | ||||
| chr12:94459833-94460007 | Common:2; Rare:49 | ||||
| chr12:95003644-95003812 | Common:3; Rare:65; Clinvar (benign):3 | ||||
| chr12:95217377-95217849 | Common:4; Rare:128 | ||||
| chr12:95474005-95474191 | Common:2; Rare:87 | ||||
| chr12:96035569-96035783 | Common:2; Rare:45 | ||||
| chr12:96400559-96400687 | Rare:60 | ||||
| chr12:96907172-96907290 | Rare:41 |