| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6375297-6375575 | Common:3; Rare:65; Clinvar:1; Clinvar (benign):3 | ||||
| chr12:6383995-6384348 | Common:2; Rare:85 | ||||
| chr12:6384356-6384452 | Rare:22 | ||||
| chr12:6451785-6452174 | Common:4; Rare:72 | ||||
| chr12:6470672-6470745 | Rare:23 | ||||
| chr12:6493088-6493381 | Common:7; Rare:87 | ||||
| chr12:6493790-6494140 | Common:2; Rare:105 | ||||
| chr12:6534631-6534860 | Common:3; Rare:94 | ||||
| chr12:6536526-6536790 | Rare:91 | ||||
| chr12:6568216-6568384 | Rare:62 | ||||
| chr12:6598095-6598313 | Common:1; Rare:54 | ||||
| chr12:6635922-6636093 | Common:2; Rare:47 | ||||
| chr12:6688900-6689148 | Rare:79 | ||||
| chr12:6689421-6689732 | Common:2; Rare:82 | ||||
| chr12:6723844-6724296 | Common:1; Rare:97 |