| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:218398093-218398251 | Common:2; Rare:104 | ||||
| chr2:218398370-218398818 | Common:11; Rare:268 | ||||
| chr2:218399668-218400152 | Rare:357 | ||||
| chr2:218400281-218400612 | Common:14; Rare:182 | ||||
| chr2:218400898-218401229 | Common:14; Rare:195 | ||||
| chr2:218568220-218568704 | Common:10; Rare:227 | ||||
| chr2:218568733-218568973 | Common:2; Rare:113 | ||||
| chr2:218659280-218659823 | Common:8; Rare:247 | ||||
| chr2:218671939-218672372 | Common:4; Rare:221 | ||||
| chr2:218710707-218711019 | Common:4; Rare:145 | ||||
| chr2:218745000-218745547 | Common:8; Rare:201 | ||||
| chr2:218748982-218749137 | Common:2; Rare:40 | ||||
| chr2:218781352-218781978 | Common:5; Rare:169; Clinvar:4; Clinvar (benign):2 | ||||
| chr2:218781985-218782384 | Rare:231; Clinvar:24; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr2:218782410-218782760 | Common:4; Rare:99; Clinvar:2; Clinvar (benign):1 |