| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:52367257-52367308 | Common:1; Rare:17 | ||||
| chr12:52451512-52451638 | Common:1; Rare:48; Clinvar (pathogenic):1 | ||||
| chr12:52451661-52451961 | Common:4; Rare:101; Clinvar (benign):1 | ||||
| chr12:52473803-52473974 | Common:2; Rare:44 | ||||
| chr12:52492647-52492939 | Common:4; Rare:102; Clinvar:2; Clinvar (pathogenic):3 | ||||
| chr12:52517358-52518015 | Common:2; Rare:169; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr12:52518702-52519189 | Common:6; Rare:129; Clinvar:2; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr12:52519535-52520416 | Common:9; Rare:277; Clinvar:12; Clinvar (benign):12; Clinvar (pathogenic):4 | ||||
| chr12:52520419-52520609 | Common:1; Rare:36; Clinvar (benign):1 | ||||
| chr12:52552637-52552742 | Common:2; Rare:36 | ||||
| chr12:52651528-52652219 | Common:9; Rare:285; Clinvar:2; Clinvar (benign):10 | ||||
| chr12:52677876-52678254 | Common:2; Rare:91 | ||||
| chr12:52679524-52680072 | Common:3; Rare:143; Clinvar:4 | ||||
| chr12:52848548-52848687 | Common:3; Rare:36 | ||||
| chr12:52848781-52849090 | Common:3; Rare:94 |