| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:108730596-108730705 | Rare:21 | ||||
| chr12:108730781-108730870 | Rare:19 | ||||
| chr12:108731339-108731852 | Common:4; Rare:150 | ||||
| chr12:108731917-108732292 | Common:3; Rare:96 | ||||
| chr12:108856947-108857093 | Common:2; Rare:32 | ||||
| chr12:108857317-108857902 | Common:6; Rare:229 | ||||
| chr12:108857946-108858009 | Rare:12 | ||||
| chr12:109052427-109052791 | Common:4; Rare:109 | ||||
| chr12:109053208-109053293 | Rare:17 | ||||
| chr12:109093373-109093632 | Common:2; Rare:96 | ||||
| chr12:109097442-109097622 | Rare:62; Clinvar:1 | ||||
| chr12:109097893-109098291 | Common:5; Rare:120 | ||||
| chr12:109098323-109098580 | Rare:112; Clinvar:4; Clinvar (benign):1 | ||||
| chr12:109154525-109154726 | Common:1; Rare:55 | ||||
| chr12:109154735-109154763 | Common:1; Rare:2 |