| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6534636-6534860 | Common:3; Rare:90 | ||||
| chr12:6536491-6536801 | Rare:98 | ||||
| chr12:6568202-6568388 | Common:1; Rare:65 | ||||
| chr12:6607349-6607694 | Common:5; Rare:59 | ||||
| chr12:6635923-6636042 | Common:2; Rare:31 | ||||
| chr12:6663107-6663289 | Rare:51 | ||||
| chr12:6723968-6724172 | Rare:53 | ||||
| chr12:6724196-6724306 | Common:1; Rare:25 | ||||
| chr12:6766351-6766748 | Rare:120 | ||||
| chr12:6851921-6852221 | Rare:75 | ||||
| chr12:6867361-6867604 | Common:2; Rare:121; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:6870119-6870288 | Common:1; Rare:44; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:6873291-6873532 | Common:1; Rare:72 | ||||
| chr12:6904676-6904890 | Rare:47 | ||||
| chr12:6946347-6946635 | Common:1; Rare:71 |