| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:32399794-32399932 | Common:1; Rare:44 | ||||
| chr12:38905517-38905726 | Common:3; Rare:59 | ||||
| chr12:40224668-40225084 | Common:5; Rare:99; Clinvar (benign):1 | ||||
| chr12:42238153-42238471 | Common:1; Rare:102 | ||||
| chr12:42325922-42326223 | Common:1; Rare:92 | ||||
| chr12:43758739-43759011 | Common:2; Rare:76; Clinvar:2 | ||||
| chr12:43806229-43806385 | Common:2; Rare:54 | ||||
| chr12:45215970-45216400 | Common:2; Rare:140 | ||||
| chr12:45729447-45729747 | Common:1; Rare:84 | ||||
| chr12:45990390-45990959 | Common:2; Rare:183 | ||||
| chr12:46267328-46267497 | Common:1; Rare:37 | ||||
| chr12:46268578-46268697 | Rare:27 | ||||
| chr12:46268709-46269165 | Common:1; Rare:124 | ||||
| chr12:46372594-46372959 | Rare:140 | ||||
| chr12:47079511-47079651 | Common:1; Rare:27 |