| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:53049680-53050191 | Common:2; Rare:124 | ||||
| chr12:53066685-53066746 | Rare:14 | ||||
| chr12:53079356-53079568 | Common:2; Rare:70 | ||||
| chr12:53252009-53252208 | Common:3; Rare:78 | ||||
| chr12:53501213-53501320 | Rare:29 | ||||
| chr12:53501532-53501582 | Rare:8 | ||||
| chr12:53727415-53727712 | Rare:65 | ||||
| chr12:53984986-53985275 | Common:2; Rare:77 | ||||
| chr12:53999946-54000171 | Common:4; Rare:61 | ||||
| chr12:54009454-54009663 | Common:1; Rare:66 | ||||
| chr12:54028398-54028519 | Rare:31 | ||||
| chr12:54188955-54189149 | Rare:44 | ||||
| chr12:54588403-54588504 | Rare:21 | ||||
| chr12:55707495-55707551 | Rare:18; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:55715994-55716208 | Common:2; Rare:95 |