| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:110124750-110124938 | Rare:24 | ||||
| chr12:110280492-110280711 | Rare:56 | ||||
| chr12:110280713-110280842 | Rare:32 | ||||
| chr12:110280855-110281349 | Common:1; Rare:172; Clinvar (benign):1 | ||||
| chr12:110281545-110281748 | Common:1; Rare:56; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:110345481-110345514 | Rare:6 | ||||
| chr12:110403269-110403291 | Rare:8 | ||||
| chr12:110403347-110403543 | Common:2; Rare:45 | ||||
| chr12:110403589-110403798 | Common:2; Rare:101 | ||||
| chr12:110449820-110449963 | Common:1; Rare:28 | ||||
| chr12:110450047-110450096 | Rare:14 | ||||
| chr12:110450231-110450504 | Common:2; Rare:93 | ||||
| chr12:110468113-110468534 | Common:3; Rare:146 | ||||
| chr12:110468637-110468678 | Rare:15 | ||||
| chr12:110468711-110468941 | Rare:69 |