| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:4538436-4538807 | Rare:77 | ||||
| chr12:4649010-4649171 | Common:2; Rare:55; Clinvar (benign):2 | ||||
| chr12:6200005-6200501 | Common:4; Rare:149 | ||||
| chr12:6375207-6375667 | Common:5; Rare:116; Clinvar:1; Clinvar (benign):6 | ||||
| chr12:6376168-6376449 | Common:3; Rare:61 | ||||
| chr12:6452079-6452159 | Common:1; Rare:19 | ||||
| chr12:6493235-6493381 | Common:6; Rare:41 | ||||
| chr12:6493778-6494126 | Common:2; Rare:104 | ||||
| chr12:6534329-6534568 | Common:5; Rare:105 | ||||
| chr12:6534631-6534860 | Common:3; Rare:94 | ||||
| chr12:6568260-6568388 | Rare:50 | ||||
| chr12:6606623-6606973 | Rare:118 | ||||
| chr12:6688843-6689089 | Rare:76 | ||||
| chr12:6689437-6689732 | Common:2; Rare:73 | ||||
| chr12:6724220-6724296 | Rare:13 |