| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:10613540-10613679 | Common:1; Rare:57 | ||||
| chr12:11171595-11171666 | Common:1; Rare:19 | ||||
| chr12:14803472-14803670 | Common:1; Rare:47 | ||||
| chr12:15789352-15789597 | Rare:88 | ||||
| chr12:15882290-15882576 | Common:1; Rare:87 | ||||
| chr12:21501581-21501847 | Common:1; Rare:65 | ||||
| chr12:25195132-25195301 | Common:2; Rare:47 | ||||
| chr12:26938263-26938519 | Common:1; Rare:97 | ||||
| chr12:31959386-31959419 | Rare:6 | ||||
| chr12:42326065-42326182 | Common:1; Rare:36 | ||||
| chr12:43758721-43759007 | Common:2; Rare:85; Clinvar:2 | ||||
| chr12:43806241-43806425 | Common:2; Rare:64 | ||||
| chr12:46372740-46372975 | Rare:98 | ||||
| chr12:47705972-47706088 | Rare:55 | ||||
| chr12:49188998-49189296 | Rare:81; Clinvar:2; Clinvar (benign):2 |