| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:31326083-31326423 | Common:3; Rare:99 | ||||
| chr12:31659147-31659229 | Common:1; Rare:30 | ||||
| chr12:31728995-31729331 | Common:1; Rare:106 | ||||
| chr12:31958925-31959238 | Common:3; Rare:65 | ||||
| chr12:31959258-31959488 | Common:2; Rare:75 | ||||
| chr12:32399230-32399572 | Common:5; Rare:93 | ||||
| chr12:32399750-32400179 | Common:4; Rare:119 | ||||
| chr12:32679107-32679358 | Common:1; Rare:103; Clinvar:1; Clinvar (benign):4 | ||||
| chr12:32755853-32756028 | Common:1; Rare:63 | ||||
| chr12:32896760-32897023 | Common:3; Rare:87; Clinvar:4; Clinvar (benign):3 | ||||
| chr12:38905526-38905733 | Common:3; Rare:57 | ||||
| chr12:38905947-38906077 | Rare:31 | ||||
| chr12:38906170-38906405 | Common:1; Rare:50 | ||||
| chr12:38906713-38906841 | Common:1; Rare:26 | ||||
| chr12:38907030-38907199 | Rare:30 |