| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:108531212-108531498 | Rare:65 | ||||
| chr12:108535367-108535552 | Common:1; Rare:36 | ||||
| chr12:108561132-108561488 | Common:4; Rare:90 | ||||
| chr12:108562361-108562715 | Common:9; Rare:143; Clinvar:2; Clinvar (benign):6 | ||||
| chr12:109097867-109098335 | Common:5; Rare:145 | ||||
| chr12:109130749-109131433 | Common:3; Rare:125 | ||||
| chr12:109154557-109154875 | Common:3; Rare:72 | ||||
| chr12:109154977-109155284 | Common:2; Rare:57 | ||||
| chr12:109477275-109477650 | Common:3; Rare:95 | ||||
| chr12:109573430-109573813 | Common:3; Rare:126; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr12:109880371-109880651 | Common:1; Rare:88 | ||||
| chr12:109900159-109900302 | Rare:49 | ||||
| chr12:110502047-110502331 | Common:1; Rare:102 | ||||
| chr12:111685743-111686110 | Rare:134 | ||||
| chr12:111766847-111767093 | Rare:78 |