| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:53321232-53321429 | Common:1; Rare:71; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr12:53321470-53321628 | Common:1; Rare:53; Clinvar:3 | ||||
| chr12:53379987-53380289 | Common:4; Rare:124 | ||||
| chr12:53441484-53441777 | Common:1; Rare:76 | ||||
| chr12:53452010-53452373 | Rare:94 | ||||
| chr12:53452574-53452894 | Common:2; Rare:111 | ||||
| chr12:53493015-53493287 | Common:1; Rare:76 | ||||
| chr12:53499442-53499672 | Rare:48 | ||||
| chr12:53501198-53501352 | Rare:36 | ||||
| chr12:53501537-53501596 | Rare:11 | ||||
| chr12:53524960-53525122 | Rare:29 | ||||
| chr12:53625876-53626174 | Common:1; Rare:74 | ||||
| chr12:53626326-53626434 | Common:2; Rare:36 | ||||
| chr12:53675813-53675855 | Rare:11 | ||||
| chr12:53675860-53676467 | Common:8; Rare:243 |