| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6851922-6852182 | Rare:66 | ||||
| chr12:6852338-6852661 | Common:1; Rare:77 | ||||
| chr12:6867358-6867574 | Common:2; Rare:106; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:6970616-6970961 | Common:3; Rare:108 | ||||
| chr12:7018472-7018707 | Common:1; Rare:63 | ||||
| chr12:8697827-8698023 | Rare:80 | ||||
| chr12:10613524-10613684 | Common:1; Rare:65 | ||||
| chr12:11171609-11171646 | Common:1; Rare:9 | ||||
| chr12:12891309-12891568 | Common:1; Rare:51 | ||||
| chr12:14803438-14803710 | Common:1; Rare:70 | ||||
| chr12:15882319-15882648 | Common:1; Rare:89 | ||||
| chr12:21501556-21501889 | Common:2; Rare:86 | ||||
| chr12:25195151-25195299 | Common:1; Rare:43 | ||||
| chr12:26938276-26938541 | Common:3; Rare:99 | ||||
| chr12:27332705-27332977 | Common:2; Rare:87 |