| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:38906204-38906330 | Rare:26 | ||||
| chr12:38906697-38906810 | Common:1; Rare:27 | ||||
| chr12:39442632-39442706 | Rare:13 | ||||
| chr12:39443323-39443509 | Rare:58; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:39619732-39619919 | Common:1; Rare:32 | ||||
| chr12:40692275-40692292 | Rare:2 | ||||
| chr12:40692316-40692585 | Common:1; Rare:83 | ||||
| chr12:42238153-42238492 | Common:2; Rare:112 | ||||
| chr12:42325934-42326243 | Common:2; Rare:97 | ||||
| chr12:43552131-43552371 | Common:3; Rare:66 | ||||
| chr12:43758721-43758996 | Common:2; Rare:81; Clinvar:2 | ||||
| chr12:43806220-43806385 | Common:2; Rare:54 | ||||
| chr12:44875554-44875722 | Common:3; Rare:41 | ||||
| chr12:44876057-44876473 | Common:3; Rare:129 | ||||
| chr12:45215523-45215699 | Rare:27 |