| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:122423704-122423935 | Common:1; Rare:30 | ||||
| chr12:122756514-122756771 | Common:1; Rare:44 | ||||
| chr12:122762094-122762207 | Common:1; Rare:24 | ||||
| chr12:122763583-122763742 | Common:2; Rare:41 | ||||
| chr12:123246010-123246236 | Common:1; Rare:45 | ||||
| chr12:123363591-123363904 | Rare:77 | ||||
| chr12:123630244-123630419 | Rare:40; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr12:124387614-124387658 | Rare:6 | ||||
| chr12:124423200-124423362 | Common:1; Rare:45 | ||||
| chr12:124780136-124780327 | Common:1; Rare:40 | ||||
| chr12:130875643-130875906 | Common:2; Rare:52 | ||||
| chr12:131860861-131861209 | Common:1; Rare:72 | ||||
| chr12:132189678-132189994 | Common:7; Rare:110 | ||||
| chr13:19671630-19671896 | Common:1; Rare:54 | ||||
| chr13:29849516-29849848 | Rare:78 |