| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:46549869-46550000 | Common:1; Rare:26 | ||||
| chr12:47080798-47081056 | Common:3; Rare:77 | ||||
| chr12:47081075-47081106 | Rare:5 | ||||
| chr12:47081316-47081466 | Rare:31 | ||||
| chr12:47082823-47083064 | Common:1; Rare:49 | ||||
| chr12:47306968-47306985 | Common:1; Rare:4 | ||||
| chr12:49060784-49060903 | Common:1; Rare:48 | ||||
| chr12:52147261-52147571 | Common:2; Rare:75 | ||||
| chr12:52286792-52287321 | Common:4; Rare:144; Clinvar (pathogenic):2 | ||||
| chr12:52287857-52287950 | Common:2; Rare:24 | ||||
| chr12:56634984-56635109 | Rare:21 | ||||
| chr12:57239225-57239416 | Common:1; Rare:42 | ||||
| chr12:57935898-57936211 | Common:4; Rare:79 | ||||
| chr12:62603432-62603614 | Common:1; Rare:68 | ||||
| chr12:62703138-62703235 | Common:1; Rare:14 |