| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:122526852-122527291 | Common:4; Rare:162 | ||||
| chr12:122896048-122896212 | Rare:88 | ||||
| chr12:122974533-122974825 | Common:1; Rare:70 | ||||
| chr12:122975151-122975252 | Common:1; Rare:31 | ||||
| chr12:122980218-122980289 | Rare:25 | ||||
| chr12:122980568-122980964 | Common:2; Rare:114 | ||||
| chr12:123232745-123232917 | Common:4; Rare:45 | ||||
| chr12:123233081-123233506 | Common:3; Rare:145; Clinvar:1 | ||||
| chr12:123364824-123365005 | Common:3; Rare:66 | ||||
| chr12:123383898-123384179 | Rare:65 | ||||
| chr12:123436434-123436536 | Rare:16 | ||||
| chr12:123584307-123584637 | Common:6; Rare:120 | ||||
| chr12:123602001-123602211 | Common:3; Rare:72 | ||||
| chr12:123633546-123633886 | Common:2; Rare:162; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:123972575-123972910 | Common:6; Rare:117 |