| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:110345280-110345800 | Common:2; Rare:99; Clinvar (pathogenic):1 | ||||
| chr12:110403512-110403806 | Common:6; Rare:217 | ||||
| chr12:110404000-110404204 | Common:6; Rare:75 | ||||
| chr12:110449630-110450000 | Common:4; Rare:155 | ||||
| chr12:110450177-110450519 | Common:6; Rare:246 | ||||
| chr12:110468120-110468600 | Common:9; Rare:426 | ||||
| chr12:110468659-110468924 | Rare:163 | ||||
| chr12:110501310-110501693 | Common:3; Rare:198 | ||||
| chr12:110501946-110502359 | Common:3; Rare:372 | ||||
| chr12:110582541-110582951 | Common:2; Rare:213 | ||||
| chr12:110583224-110583514 | Rare:137 | ||||
| chr12:110613870-110614264 | Rare:252; Clinvar:8; Clinvar (benign):6 | ||||
| chr12:110742757-110743252 | Common:9; Rare:446 | ||||
| chr12:111368973-111369306 | Common:3; Rare:231 | ||||
| chr12:111405586-111406030 | Common:2; Rare:310 |