| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:57459494-57459796 | Common:3; Rare:55 | ||||
| chr12:57520399-57520727 | Common:2; Rare:91 | ||||
| chr12:57527757-57527956 | Rare:67 | ||||
| chr12:57591354-57591457 | Common:1; Rare:29 | ||||
| chr12:57694198-57694321 | Common:1; Rare:28 | ||||
| chr12:57716088-57716744 | Common:4; Rare:171 | ||||
| chr12:57744851-57745162 | Common:1; Rare:75 | ||||
| chr12:57765483-57765789 | Common:2; Rare:95 | ||||
| chr12:57772081-57772276 | Rare:63 | ||||
| chr12:57772520-57772634 | Common:2; Rare:15 | ||||
| chr12:57846930-57847221 | Common:2; Rare:108 | ||||
| chr12:58920323-58920626 | Common:2; Rare:95 | ||||
| chr12:62260040-62260498 | Common:1; Rare:168 | ||||
| chr12:62321554-62321730 | Common:1; Rare:31 | ||||
| chr12:63779657-63779934 | Common:3; Rare:96; Clinvar (benign):1 |