| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:56051401-56051857 | Common:1; Rare:173; Clinvar:5; Clinvar (benign):1 | ||||
| chr7:56106392-56106709 | Common:9; Rare:110 | ||||
| chr7:66682017-66682166 | Common:5; Rare:72 | ||||
| chr7:66921130-66921459 | Common:1; Rare:97 | ||||
| chr7:73683429-73683622 | Common:3; Rare:77 | ||||
| chr7:73738752-73739047 | Common:1; Rare:100 | ||||
| chr7:74254379-74254505 | Rare:54 | ||||
| chr7:75994498-75994774 | Common:4; Rare:137 | ||||
| chr7:76047768-76048187 | Common:3; Rare:123 | ||||
| chr7:76302775-76302931 | Rare:78; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
| chr7:76303748-76304006 | Common:2; Rare:132; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):7 | ||||
| chr7:77696257-77696467 | Rare:85 | ||||
| chr7:77798312-77798666 | Rare:61 | ||||
| chr7:87152317-87152453 | Common:1; Rare:41 | ||||
| chr7:87345455-87345757 | Common:6; Rare:97 |