| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:53295411-53295578 | Common:1; Rare:55 | ||||
| chr12:53321292-53321414 | Common:1; Rare:52; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr12:53379871-53380199 | Common:1; Rare:115 | ||||
| chr12:53441434-53441778 | Common:1; Rare:99 | ||||
| chr12:53452123-53452355 | Rare:46 | ||||
| chr12:53501189-53501320 | Rare:33 | ||||
| chr12:53501530-53501621 | Rare:22 | ||||
| chr12:53625950-53626137 | Common:1; Rare:45 | ||||
| chr12:53676056-53676302 | Common:3; Rare:110 | ||||
| chr12:53727425-53727712 | Rare:65 | ||||
| chr12:54053636-54053843 | Rare:32 | ||||
| chr12:54188968-54189172 | Rare:48 | ||||
| chr12:54279675-54279905 | Common:1; Rare:78 | ||||
| chr12:54280032-54280320 | Rare:94 | ||||
| chr12:54473560-54473662 | Common:1; Rare:24 |