| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:108561157-108561258 | Rare:34 | ||||
| chr12:108562361-108562649 | Common:5; Rare:109; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:109052491-109052638 | Common:1; Rare:36 | ||||
| chr12:109097442-109097644 | Rare:73; Clinvar:2 | ||||
| chr12:109097955-109098223 | Common:5; Rare:87 | ||||
| chr12:109477297-109477662 | Common:3; Rare:86 | ||||
| chr12:109573472-109573840 | Common:3; Rare:108; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr12:109880381-109880668 | Common:1; Rare:87 | ||||
| chr12:110403607-110403782 | Common:2; Rare:93 | ||||
| chr12:110450254-110450464 | Common:2; Rare:78 | ||||
| chr12:110468667-110468914 | Rare:61 | ||||
| chr12:110502065-110502156 | Common:1; Rare:38 | ||||
| chr12:110614011-110614210 | Rare:61; Clinvar:3; Clinvar (benign):2 | ||||
| chr12:110742862-110743183 | Common:2; Rare:114 | ||||
| chr12:111685761-111686114 | Rare:131 |