| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:30695717-30696034 | Common:5; Rare:85 | ||||
| chr12:30754749-30755078 | Common:1; Rare:133 | ||||
| chr12:31073716-31073908 | Common:8; Rare:67 | ||||
| chr12:31074089-31074271 | Common:1; Rare:37 | ||||
| chr12:31324064-31324251 | Rare:52 | ||||
| chr12:31325857-31326080 | Common:2; Rare:40 | ||||
| chr12:31326084-31326451 | Common:4; Rare:126 | ||||
| chr12:31590992-31591292 | Common:1; Rare:126 | ||||
| chr12:31659131-31659245 | Common:1; Rare:37 | ||||
| chr12:31728993-31729377 | Common:1; Rare:120 | ||||
| chr12:31959262-31959488 | Common:2; Rare:73 | ||||
| chr12:32106663-32106936 | Common:5; Rare:78 | ||||
| chr12:32679091-32679357 | Common:1; Rare:105; Clinvar:1; Clinvar (benign):4 | ||||
| chr12:32679546-32679741 | Rare:49 | ||||
| chr12:32755237-32755319 | Common:1; Rare:22; Clinvar:2; Clinvar (pathogenic):1 |