| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6534355-6534569 | Common:5; Rare:93 | ||||
| chr12:6568237-6568371 | Rare:51 | ||||
| chr12:6635957-6636077 | Common:2; Rare:34 | ||||
| chr12:6663089-6663403 | Common:2; Rare:89 | ||||
| chr12:6688870-6689227 | Rare:109 | ||||
| chr12:6723844-6724177 | Common:1; Rare:72 | ||||
| chr12:6724196-6724296 | Rare:21 | ||||
| chr12:6752938-6753189 | Common:6; Rare:77 | ||||
| chr12:6851902-6852180 | Rare:73 | ||||
| chr12:6867365-6867611 | Common:2; Rare:121; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:6873282-6873534 | Common:2; Rare:73 | ||||
| chr12:6904679-6904839 | Rare:38 | ||||
| chr12:6943531-6943829 | Common:4; Rare:129 | ||||
| chr12:6970621-6970977 | Common:4; Rare:115; Clinvar (benign):1 | ||||
| chr12:7108481-7108681 | Common:1; Rare:58 |