| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:64794244-64794476 | Common:7; Rare:125 | ||||
| chr7:65006630-65006900 | Common:6; Rare:151 | ||||
| chr7:65373674-65373949 | Rare:147 | ||||
| chr7:65982100-65982353 | Common:6; Rare:153; Clinvar:6; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr7:66075597-66075992 | Rare:199; Clinvar (benign):2 | ||||
| chr7:66114732-66114902 | Common:3; Rare:144 | ||||
| chr7:66115172-66115380 | Common:1; Rare:90 | ||||
| chr7:66204963-66205390 | Common:1; Rare:129 | ||||
| chr7:66628612-66629007 | Common:5; Rare:241; Clinvar:8 | ||||
| chr7:66682000-66682229 | Common:12; Rare:205 | ||||
| chr7:66740320-66741320 | Common:11; Rare:354 | ||||
| chr7:66921065-66921358 | Common:1; Rare:174 | ||||
| chr7:66996553-66996932 | Common:5; Rare:157 | ||||
| chr7:72828128-72828691 | Common:7; Rare:331 | ||||
| chr7:72879225-72879449 | Common:7; Rare:155 |