| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:93441859-93442374 | Common:6; Rare:179 | ||||
| chr12:93570827-93571285 | Common:1; Rare:105 | ||||
| chr12:93571731-93571912 | Common:7; Rare:69 | ||||
| chr12:93572569-93572837 | Common:1; Rare:85 | ||||
| chr12:93677253-93677400 | Rare:34 | ||||
| chr12:94459798-94460080 | Common:3; Rare:82 | ||||
| chr12:94616070-94616215 | Rare:29 | ||||
| chr12:95003593-95003831 | Common:3; Rare:99; Clinvar (benign):6 | ||||
| chr12:95217376-95217890 | Common:4; Rare:136 | ||||
| chr12:95218165-95218316 | Common:2; Rare:36 | ||||
| chr12:95474039-95474281 | Common:2; Rare:110 | ||||
| chr12:95548796-95548903 | Common:2; Rare:40 | ||||
| chr12:95858806-95859081 | Common:3; Rare:82 | ||||
| chr12:96035354-96035452 | Common:1; Rare:27 | ||||
| chr12:96035527-96035735 | Common:2; Rare:44 |