| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:49018741-49019120 | Common:1; Rare:126; Clinvar (benign):1 | ||||
| chr12:49264756-49265095 | Common:4; Rare:120 | ||||
| chr12:49568104-49568246 | Common:2; Rare:44 | ||||
| chr12:49828392-49828594 | Common:1; Rare:72 | ||||
| chr12:50222456-50222710 | Common:1; Rare:59 | ||||
| chr12:50283478-50283654 | Common:1; Rare:57 | ||||
| chr12:51270260-51270299 | Rare:10 | ||||
| chr12:51270301-51270357 | Common:2; Rare:16 | ||||
| chr12:52949826-52949985 | Rare:36 | ||||
| chr12:53047033-53047240 | Common:1; Rare:48 | ||||
| chr12:53049884-53050076 | Rare:48 | ||||
| chr12:53097303-53097678 | Common:1; Rare:73 | ||||
| chr12:53097821-53098227 | Common:1; Rare:106 | ||||
| chr12:53299436-53299702 | Common:2; Rare:72 | ||||
| chr12:55716020-55716109 | Common:1; Rare:44 |