| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6935446-6935645 | Common:1; Rare:53 | ||||
| chr12:6957801-6958065 | Rare:78 | ||||
| chr12:6962338-6962600 | Common:4; Rare:48 | ||||
| chr12:6963049-6963277 | Common:1; Rare:51 | ||||
| chr12:6964019-6964175 | Common:1; Rare:53 | ||||
| chr12:6974137-6974403 | Rare:76 | ||||
| chr12:6992949-6993040 | Rare:18 | ||||
| chr12:7014050-7014094 | Common:1; Rare:7 | ||||
| chr12:7088589-7088934 | Common:1; Rare:106; Clinvar (pathogenic):2 | ||||
| chr12:7089286-7089735 | Common:3; Rare:145 | ||||
| chr12:7111337-7111505 | Rare:35 | ||||
| chr12:7117209-7117504 | Common:1; Rare:46 | ||||
| chr12:7118223-7118282 | Rare:6 | ||||
| chr12:8026535-8026838 | Common:1; Rare:78 | ||||
| chr12:8242933-8243249 | Common:8; Rare:89 |