| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:53295442-53295586 | Common:1; Rare:51 | ||||
| chr12:53321242-53321414 | Common:1; Rare:63; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr12:53441510-53441768 | Common:1; Rare:64 | ||||
| chr12:53499449-53499697 | Rare:55 | ||||
| chr12:53501047-53501352 | Rare:75 | ||||
| chr12:53626308-53626533 | Common:3; Rare:57 | ||||
| chr12:53676035-53676123 | Rare:52 | ||||
| chr12:53984983-53985267 | Common:2; Rare:73 | ||||
| chr12:53999946-54000075 | Common:4; Rare:39 | ||||
| chr12:54016641-54016899 | Rare:61 | ||||
| chr12:54017117-54017190 | Common:1; Rare:12 | ||||
| chr12:54385709-54385905 | Rare:39 | ||||
| chr12:55712110-55712402 | Common:6; Rare:73 | ||||
| chr12:55716014-55716195 | Common:1; Rare:85 | ||||
| chr12:55716324-55716548 | Common:2; Rare:59 |