| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:15789290-15789617 | Common:1; Rare:113 | ||||
| chr12:15882319-15882657 | Common:1; Rare:95 | ||||
| chr12:21437616-21437717 | Common:4; Rare:43 | ||||
| chr12:21501556-21501880 | Common:2; Rare:84 | ||||
| chr12:21526197-21526317 | Rare:15 | ||||
| chr12:21657765-21657997 | Common:4; Rare:80; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:22544488-22544669 | Common:1; Rare:40 | ||||
| chr12:22625019-22625244 | Rare:116 | ||||
| chr12:24902044-24902302 | Common:3; Rare:60 | ||||
| chr12:25195158-25195308 | Common:1; Rare:47 | ||||
| chr12:26630670-26630806 | Rare:27 | ||||
| chr12:26937937-26938534 | Common:11; Rare:195 | ||||
| chr12:27244064-27244321 | Common:2; Rare:79 | ||||
| chr12:27523990-27524326 | Rare:76 | ||||
| chr12:27710755-27710923 | Common:2; Rare:81 |