| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6581039-6581388 | Rare:120; Clinvar (pathogenic):2 | ||||
| chr12:6607874-6607934 | Rare:9 | ||||
| chr12:6688768-6689013 | Rare:53 | ||||
| chr12:6689057-6689169 | Rare:34 | ||||
| chr12:6689220-6689756 | Common:3; Rare:145 | ||||
| chr12:6699959-6700144 | Rare:53 | ||||
| chr12:6723847-6724316 | Common:2; Rare:100 | ||||
| chr12:6753038-6753223 | Common:4; Rare:64 | ||||
| chr12:6765158-6765511 | Rare:51 | ||||
| chr12:6766090-6766747 | Common:1; Rare:171 | ||||
| chr12:6768934-6769173 | Common:2; Rare:44 | ||||
| chr12:6821713-6821878 | Common:1; Rare:44 | ||||
| chr12:6827998-6828249 | Common:4; Rare:42 | ||||
| chr12:6828354-6828443 | Common:3; Rare:21 | ||||
| chr12:6829636-6829779 | Common:1; Rare:24 |