| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:57941360-57941661 | Common:3; Rare:89 | ||||
| chr12:59595934-59596176 | Common:5; Rare:62 | ||||
| chr12:62260165-62260417 | Common:1; Rare:91 | ||||
| chr12:63780085-63780175 | Rare:41; Clinvar (pathogenic):1 | ||||
| chr12:64222248-64222355 | Rare:35 | ||||
| chr12:64452011-64452171 | Common:1; Rare:60 | ||||
| chr12:64759373-64759668 | Common:3; Rare:87; Clinvar:3 | ||||
| chr12:65824823-65824833 | Rare:2 | ||||
| chr12:65824947-65825122 | Rare:44 | ||||
| chr12:66130703-66130809 | Rare:40 | ||||
| chr12:66169941-66170074 | Common:1; Rare:39 | ||||
| chr12:68332265-68332527 | Common:1; Rare:86 | ||||
| chr12:68610716-68611041 | Common:1; Rare:135 | ||||
| chr12:68686803-68687034 | Common:5; Rare:73 | ||||
| chr12:68808847-68809034 | Rare:35 |