| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:54419453-54419663 | Rare:36 | ||||
| chr12:55715996-55716195 | Common:2; Rare:93 | ||||
| chr12:55716734-55716961 | Rare:51 | ||||
| chr12:55726918-55727287 | Common:2; Rare:121 | ||||
| chr12:55728275-55728514 | Rare:77 | ||||
| chr12:55728952-55729133 | Rare:33 | ||||
| chr12:55729657-55729801 | Rare:32 | ||||
| chr12:55829500-55829793 | Rare:92 | ||||
| chr12:55830752-55830937 | Rare:58 | ||||
| chr12:55842928-55843086 | Rare:34 | ||||
| chr12:55930969-55931215 | Common:1; Rare:38 | ||||
| chr12:55931894-55932116 | Rare:54 | ||||
| chr12:55966697-55966863 | Rare:42 | ||||
| chr12:56041689-56041972 | Common:3; Rare:70; Clinvar (benign):1 | ||||
| chr12:56079738-56080221 | Common:4; Rare:110 |