| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:57243345-57243599 | Common:1; Rare:57 | ||||
| chr12:57243709-57243818 | Common:1; Rare:46; Clinvar (benign):1 | ||||
| chr12:57245119-57245232 | Common:1; Rare:38; Clinvar (benign):1 | ||||
| chr12:57280285-57280464 | Common:1; Rare:36 | ||||
| chr12:57459130-57459382 | Common:1; Rare:47 | ||||
| chr12:57462357-57462528 | Rare:63 | ||||
| chr12:57462711-57462906 | Common:1; Rare:48 | ||||
| chr12:57726155-57726308 | Rare:44 | ||||
| chr12:57726641-57726763 | Rare:19 | ||||
| chr12:57764720-57764924 | Common:1; Rare:60; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr12:57844689-57844858 | Rare:28 | ||||
| chr12:57865110-57865275 | Common:1; Rare:39 | ||||
| chr12:57865338-57865512 | Rare:40 | ||||
| chr12:57865609-57865709 | Rare:18 | ||||
| chr12:57905340-57905670 | Common:1; Rare:43 |