| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6723970-6724142 | Rare:42 | ||||
| chr12:6753055-6753180 | Common:4; Rare:44 | ||||
| chr12:6821542-6821883 | Common:3; Rare:85 | ||||
| chr12:6851890-6852195 | Rare:79 | ||||
| chr12:6867384-6867555 | Common:2; Rare:77; Clinvar:1; Clinvar (benign):2 | ||||
| chr12:6873297-6873544 | Common:1; Rare:73 | ||||
| chr12:6904693-6904839 | Rare:36 | ||||
| chr12:6914369-6914621 | Rare:61 | ||||
| chr12:6970628-6970955 | Common:3; Rare:102 | ||||
| chr12:7189551-7189723 | Rare:64; Clinvar:4 | ||||
| chr12:8032589-8032775 | Rare:65 | ||||
| chr12:8696974-8697305 | Common:2; Rare:80 | ||||
| chr12:8697669-8698167 | Common:4; Rare:171 | ||||
| chr12:8914366-8914763 | Common:6; Rare:115 | ||||
| chr12:8949608-8949849 | Common:1; Rare:47 |