| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:96035299-96035422 | Rare:31 | ||||
| chr12:96035475-96035795 | Common:2; Rare:79 | ||||
| chr12:96399323-96399828 | Common:2; Rare:148 | ||||
| chr12:96400292-96400721 | Common:2; Rare:163 | ||||
| chr12:96907064-96907390 | Common:3; Rare:115 | ||||
| chr12:98515261-98515817 | Common:1; Rare:187; Clinvar:5 | ||||
| chr12:98516118-98516580 | Common:4; Rare:153; Clinvar:1 | ||||
| chr12:98593390-98593792 | Common:2; Rare:137; Clinvar:4; Clinvar (benign):4 | ||||
| chr12:98644425-98644822 | Common:3; Rare:142 | ||||
| chr12:98645013-98645362 | Common:2; Rare:104 | ||||
| chr12:100142088-100142481 | Common:2; Rare:96 | ||||
| chr12:100142772-100143093 | Common:3; Rare:122 | ||||
| chr12:100199481-100199500 | Rare:2 | ||||
| chr12:100199699-100200133 | Common:3; Rare:96 | ||||
| chr12:100200704-100200864 | Rare:52 |