| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:89524725-89524869 | Common:1; Rare:28 | ||||
| chr12:89525428-89525612 | Common:1; Rare:43 | ||||
| chr12:89525995-89526021 | Rare:13 | ||||
| chr12:89526022-89526033 | Rare:3 | ||||
| chr12:89708819-89709099 | Common:1; Rare:108 | ||||
| chr12:92145807-92146083 | Common:4; Rare:93 | ||||
| chr12:92929281-92929513 | Rare:68 | ||||
| chr12:93377728-93377929 | Rare:54 | ||||
| chr12:93441888-93442164 | Common:2; Rare:87 | ||||
| chr12:93570827-93571075 | Rare:64 | ||||
| chr12:93571755-93571912 | Common:7; Rare:61 | ||||
| chr12:94459798-94460045 | Common:3; Rare:69 | ||||
| chr12:95003627-95003788 | Common:3; Rare:66; Clinvar (benign):4 | ||||
| chr12:95073403-95073653 | Common:2; Rare:85 | ||||
| chr12:95217378-95217835 | Common:4; Rare:124 |