| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:56007583-56007889 | Common:2; Rare:79 | ||||
| chr12:56041599-56042242 | Common:6; Rare:186; Clinvar:3; Clinvar (benign):6 | ||||
| chr12:56042367-56042578 | Rare:61; Clinvar (benign):1 | ||||
| chr12:56079326-56079581 | Rare:48 | ||||
| chr12:56079674-56079884 | Rare:47 | ||||
| chr12:56079926-56080234 | Common:4; Rare:72 | ||||
| chr12:56080306-56080472 | Common:1; Rare:48 | ||||
| chr12:56104111-56104250 | Common:1; Rare:39 | ||||
| chr12:56104361-56104694 | Common:5; Rare:118 | ||||
| chr12:56116034-56116090 | Rare:10 | ||||
| chr12:56116272-56116717 | Common:3; Rare:159 | ||||
| chr12:56117900-56118420 | Common:1; Rare:153 | ||||
| chr12:56118435-56118592 | Common:1; Rare:23 | ||||
| chr12:56127833-56128336 | Rare:101 | ||||
| chr12:56128485-56128611 | Rare:34 |