| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:93377728-93377929 | Rare:54 | ||||
| chr12:93441871-93442164 | Common:2; Rare:93 | ||||
| chr12:93570875-93571075 | Rare:52 | ||||
| chr12:93571734-93571912 | Common:7; Rare:67 | ||||
| chr12:94459781-94460053 | Common:3; Rare:79 | ||||
| chr12:95003593-95003820 | Common:3; Rare:94; Clinvar (benign):6 | ||||
| chr12:95073439-95073644 | Common:1; Rare:77 | ||||
| chr12:95217347-95217840 | Common:6; Rare:131 | ||||
| chr12:95218160-95218261 | Common:2; Rare:25 | ||||
| chr12:95474014-95474330 | Common:2; Rare:134 | ||||
| chr12:95548788-95548903 | Common:2; Rare:40 | ||||
| chr12:96400527-96400677 | Common:1; Rare:69 | ||||
| chr12:96907139-96907295 | Common:1; Rare:55 | ||||
| chr12:98515478-98515881 | Rare:141; Clinvar:5; Clinvar (benign):1 | ||||
| chr12:98593464-98593776 | Common:2; Rare:101; Clinvar:4; Clinvar (benign):4 |