| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:118052514-118052710 | Common:2; Rare:30 | ||||
| chr12:118061044-118061280 | Common:1; Rare:67 | ||||
| chr12:118103798-118104151 | Common:2; Rare:82 | ||||
| chr12:118135938-118136277 | Common:2; Rare:102 | ||||
| chr12:118372820-118373183 | Common:2; Rare:97 | ||||
| chr12:120116734-120116935 | Common:2; Rare:66 | ||||
| chr12:120194697-120194760 | Rare:25 | ||||
| chr12:120200798-120200955 | Rare:49 | ||||
| chr12:120201085-120201372 | Common:2; Rare:89 | ||||
| chr12:120224697-120224823 | Common:2; Rare:41 | ||||
| chr12:120225993-120226071 | Common:1; Rare:11 | ||||
| chr12:120437838-120438265 | Common:3; Rare:157; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr12:120446353-120446491 | Common:2; Rare:64 | ||||
| chr12:120469597-120469873 | Common:2; Rare:99 | ||||
| chr12:120495859-120496227 | Common:7; Rare:124 |