| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:42299475-42299676 | Rare:33 | ||||
| chr12:42469373-42469731 | Common:3; Rare:72; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr12:43338275-43338482 | Common:3; Rare:45 | ||||
| chr12:45257151-45257248 | Rare:15 | ||||
| chr12:45726886-45727065 | Common:1; Rare:38 | ||||
| chr12:45727258-45728079 | Common:2; Rare:264 | ||||
| chr12:45728711-45728870 | Common:1; Rare:37 | ||||
| chr12:45730711-45731074 | Common:2; Rare:58 | ||||
| chr12:45732398-45732450 | Rare:10 | ||||
| chr12:45989742-45989938 | Common:1; Rare:45 | ||||
| chr12:46108767-46109040 | Common:1; Rare:42 | ||||
| chr12:46177157-46177323 | Rare:35 | ||||
| chr12:46177900-46178088 | Common:1; Rare:44 | ||||
| chr12:46210019-46210207 | Common:2; Rare:44 | ||||
| chr12:46215122-46215197 | Rare:10 |