| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:12611799-12611928 | Common:1; Rare:38 | ||||
| chr12:12717244-12717496 | Rare:83; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:12725088-12725458 | Common:3; Rare:98 | ||||
| chr12:12725642-12725951 | Common:3; Rare:71 | ||||
| chr12:12891306-12891571 | Common:1; Rare:53 | ||||
| chr12:13000166-13000481 | Common:2; Rare:97 | ||||
| chr12:13196444-13196861 | Common:1; Rare:71 | ||||
| chr12:14365482-14365736 | Common:1; Rare:88 | ||||
| chr12:14771117-14771264 | Rare:54 | ||||
| chr12:14774184-14774483 | Common:3; Rare:76 | ||||
| chr12:14803426-14803720 | Common:1; Rare:80 | ||||
| chr12:15789239-15789513 | Common:1; Rare:84 | ||||
| chr12:15882272-15882686 | Common:1; Rare:137 | ||||
| chr12:15911183-15911392 | Common:5; Rare:76 | ||||
| chr12:21437592-21437725 | Common:5; Rare:57 |