| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:53006092-53006495 | Common:4; Rare:149 | ||||
| chr12:53047020-53047072 | Rare:11 | ||||
| chr12:53049861-53050085 | Rare:56 | ||||
| chr12:53079315-53079568 | Common:2; Rare:84 | ||||
| chr12:53097311-53097700 | Common:1; Rare:81 | ||||
| chr12:53098003-53098237 | Common:1; Rare:66 | ||||
| chr12:53180588-53180789 | Common:1; Rare:77 | ||||
| chr12:53295473-53295618 | Common:1; Rare:56 | ||||
| chr12:53299415-53299722 | Common:2; Rare:86 | ||||
| chr12:53299790-53300244 | Rare:181 | ||||
| chr12:53321149-53321642 | Common:3; Rare:158; Clinvar:5; Clinvar (pathogenic):2 | ||||
| chr12:53380482-53380847 | Rare:121 | ||||
| chr12:53441454-53441799 | Common:1; Rare:99 | ||||
| chr12:53451731-53452126 | Rare:95 | ||||
| chr12:53452252-53452373 | Rare:20 |