| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:31959269-31959482 | Common:2; Rare:70 | ||||
| chr12:32896574-32896990 | Common:4; Rare:135; Clinvar:10; Clinvar (benign):10; Clinvar (pathogenic):2 | ||||
| chr12:38905573-38905700 | Common:3; Rare:34 | ||||
| chr12:39619732-39619919 | Common:1; Rare:32 | ||||
| chr12:42326004-42326215 | Common:1; Rare:68 | ||||
| chr12:43758721-43759007 | Common:2; Rare:85; Clinvar:2 | ||||
| chr12:45215987-45216163 | Common:1; Rare:58 | ||||
| chr12:45990446-45990966 | Common:3; Rare:167 | ||||
| chr12:46268578-46268684 | Rare:23 | ||||
| chr12:46269091-46269244 | Common:1; Rare:30 | ||||
| chr12:46372719-46372933 | Rare:96 | ||||
| chr12:47079519-47079637 | Common:1; Rare:23 | ||||
| chr12:47705978-47706088 | Rare:53 | ||||
| chr12:47753653-47753941 | Common:1; Rare:48 | ||||
| chr12:47758441-47758549 | Rare:24 |