| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:120495852-120496139 | Common:4; Rare:92 | ||||
| chr12:121802911-121803088 | Rare:46 | ||||
| chr12:121888623-121888859 | Common:2; Rare:76 | ||||
| chr12:122526908-122527249 | Common:3; Rare:110 | ||||
| chr12:122975129-122975314 | Common:1; Rare:71 | ||||
| chr12:122980412-122980785 | Common:1; Rare:130 | ||||
| chr12:123233109-123233512 | Common:2; Rare:134; Clinvar:1 | ||||
| chr12:123383950-123384189 | Rare:60 | ||||
| chr12:123584297-123584583 | Common:6; Rare:76 | ||||
| chr12:123584755-123584806 | Common:1; Rare:14 | ||||
| chr12:123633566-123633845 | Common:1; Rare:135; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:123972543-123972887 | Common:6; Rare:118 | ||||
| chr12:128823961-128824092 | Rare:39 | ||||
| chr12:131929046-131929300 | Common:10; Rare:77; Clinvar:1 | ||||
| chr12:132144309-132144489 | Rare:73 |