| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:89525992-89526043 | Rare:25 | ||||
| chr12:89708420-89708626 | Rare:53 | ||||
| chr12:89708757-89709085 | Common:1; Rare:123 | ||||
| chr12:89709228-89709429 | Common:3; Rare:86 | ||||
| chr12:91111396-91111623 | Common:4; Rare:51 | ||||
| chr12:92145822-92146205 | Common:2; Rare:121 | ||||
| chr12:93377728-93377929 | Rare:54 | ||||
| chr12:93441863-93442159 | Common:2; Rare:92 | ||||
| chr12:93467421-93467554 | Common:1; Rare:42 | ||||
| chr12:93571728-93571900 | Common:6; Rare:65 | ||||
| chr12:93677287-93677399 | Rare:22 | ||||
| chr12:94459832-94460047 | Common:2; Rare:63 | ||||
| chr12:95003593-95003815 | Common:3; Rare:93; Clinvar (benign):6 | ||||
| chr12:95217377-95217746 | Common:4; Rare:100 | ||||
| chr12:95218140-95218303 | Common:2; Rare:44 |