| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:10613534-10613694 | Common:1; Rare:65 | ||||
| chr12:10674064-10674151 | Rare:19 | ||||
| chr12:11171139-11171249 | Rare:42 | ||||
| chr12:11171567-11171782 | Common:6; Rare:72 | ||||
| chr12:12356980-12357201 | Common:4; Rare:112 | ||||
| chr12:12611785-12612092 | Common:2; Rare:84 | ||||
| chr12:12684458-12684649 | Common:2; Rare:27 | ||||
| chr12:12696646-12696744 | Rare:33 | ||||
| chr12:12717207-12717497 | Rare:99; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:12725649-12725929 | Common:2; Rare:60 | ||||
| chr12:12785590-12785660 | Rare:12 | ||||
| chr12:13000086-13000486 | Common:2; Rare:124 | ||||
| chr12:13044325-13044406 | Rare:24 | ||||
| chr12:13980377-13981016 | Common:3; Rare:148 | ||||
| chr12:13981524-13981679 | Common:2; Rare:26 |