| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:57818628-57818747 | Common:1; Rare:32 | ||||
| chr12:57846906-57847221 | Common:2; Rare:113 | ||||
| chr12:57941360-57941688 | Common:3; Rare:96 | ||||
| chr12:58920491-58920672 | Common:2; Rare:67 | ||||
| chr12:59595904-59596196 | Common:5; Rare:69 | ||||
| chr12:59597047-59597257 | Rare:57 | ||||
| chr12:62260041-62260445 | Common:1; Rare:152 | ||||
| chr12:62260904-62260993 | Rare:16 | ||||
| chr12:62467176-62467285 | Rare:29 | ||||
| chr12:63151014-63151126 | Common:1; Rare:22 | ||||
| chr12:63151173-63151311 | Common:1; Rare:23 | ||||
| chr12:63779758-63779926 | Common:2; Rare:59; Clinvar (benign):1 | ||||
| chr12:63779951-63780169 | Common:1; Rare:97; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):3 | ||||
| chr12:63843665-63843929 | Common:2; Rare:77 | ||||
| chr12:63844635-63844759 | Rare:27 |