| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6534585-6534860 | Common:3; Rare:109 | ||||
| chr12:6568280-6568391 | Rare:42 | ||||
| chr12:6689460-6689732 | Common:2; Rare:68 | ||||
| chr12:6723854-6724151 | Common:1; Rare:57 | ||||
| chr12:6724196-6724285 | Rare:19 | ||||
| chr12:6766321-6766748 | Rare:128 | ||||
| chr12:6851269-6851504 | Rare:50 | ||||
| chr12:6867355-6867594 | Common:2; Rare:120; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:6914355-6914555 | Rare:47 | ||||
| chr12:6970646-6970955 | Common:3; Rare:96 | ||||
| chr12:7109236-7109499 | Common:1; Rare:60 | ||||
| chr12:7189551-7189715 | Rare:59; Clinvar:3 | ||||
| chr12:8697794-8698049 | Rare:105 | ||||
| chr12:8914374-8914739 | Common:6; Rare:106 | ||||
| chr12:10613540-10613666 | Common:1; Rare:51 |