| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:53727425-53727648 | Rare:51 | ||||
| chr12:54000010-54000089 | Rare:21 | ||||
| chr12:54259286-54259334 | Rare:6 | ||||
| chr12:54259526-54259676 | Rare:30 | ||||
| chr12:54279688-54279909 | Common:1; Rare:72 | ||||
| chr12:54280070-54280279 | Rare:77 | ||||
| chr12:54385740-54385922 | Rare:35 | ||||
| chr12:55715997-55716186 | Common:2; Rare:90 | ||||
| chr12:55716403-55716563 | Common:2; Rare:42 | ||||
| chr12:55728939-55729236 | Rare:65 | ||||
| chr12:55729665-55729794 | Rare:30 | ||||
| chr12:55829511-55829793 | Rare:92 | ||||
| chr12:55830754-55830885 | Rare:50 | ||||
| chr12:56007617-56007837 | Common:2; Rare:51 | ||||
| chr12:56041614-56041968 | Common:4; Rare:83; Clinvar (benign):1 |