| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:12611687-12612047 | Common:2; Rare:106 | ||||
| chr12:12717228-12717480 | Rare:87; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:12725659-12725929 | Common:2; Rare:58 | ||||
| chr12:12891271-12891567 | Common:1; Rare:60 | ||||
| chr12:13000212-13000453 | Common:1; Rare:80 | ||||
| chr12:14365492-14365719 | Common:1; Rare:74 | ||||
| chr12:14567687-14567889 | Common:2; Rare:45 | ||||
| chr12:14771100-14771221 | Rare:51 | ||||
| chr12:14774184-14774477 | Common:3; Rare:76 | ||||
| chr12:14803443-14803699 | Common:1; Rare:65 | ||||
| chr12:14961551-14961863 | Common:3; Rare:77 | ||||
| chr12:15882319-15882422 | Rare:34 | ||||
| chr12:16606465-16606675 | Rare:50 | ||||
| chr12:18261340-18261518 | Common:1; Rare:33 | ||||
| chr12:21437592-21437718 | Common:5; Rare:54 |