| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:108514965-108515387 | Common:1; Rare:128 | ||||
| chr12:108515585-108515783 | Common:1; Rare:37 | ||||
| chr12:108515807-108515861 | Common:1; Rare:11 | ||||
| chr12:108516609-108516621 | Rare:2 | ||||
| chr12:108560800-108560940 | Rare:51 | ||||
| chr12:108561084-108561273 | Common:1; Rare:71 | ||||
| chr12:108561400-108561494 | Common:2; Rare:20 | ||||
| chr12:108562003-108562125 | Common:3; Rare:14 | ||||
| chr12:108562310-108562685 | Common:11; Rare:143; Clinvar:2; Clinvar (benign):6 | ||||
| chr12:108562936-108563105 | Rare:40 | ||||
| chr12:108632027-108632221 | Common:1; Rare:51 | ||||
| chr12:108696135-108696292 | Common:1; Rare:21 | ||||
| chr12:108696449-108696868 | Common:1; Rare:78 | ||||
| chr12:108700995-108701302 | Common:2; Rare:65 | ||||
| chr12:108730400-108730547 | Common:1; Rare:44 |