| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:56106389-56106720 | Common:9; Rare:116 | ||||
| chr7:64563032-64563252 | Common:3; Rare:60 | ||||
| chr7:64794103-64794471 | Common:5; Rare:85 | ||||
| chr7:66075577-66075887 | Rare:85; Clinvar (benign):1 | ||||
| chr7:66114764-66114960 | Common:1; Rare:90 | ||||
| chr7:66115186-66115354 | Rare:38 | ||||
| chr7:66628691-66628983 | Common:2; Rare:108; Clinvar:5 | ||||
| chr7:66682028-66682175 | Common:5; Rare:71 | ||||
| chr7:66921149-66921424 | Common:1; Rare:84 | ||||
| chr7:66996520-66996877 | Common:4; Rare:83 | ||||
| chr7:73308780-73308890 | Rare:45 | ||||
| chr7:73578531-73578827 | Common:9; Rare:102 | ||||
| chr7:73683396-73683622 | Common:3; Rare:93 | ||||
| chr7:73738774-73739017 | Common:1; Rare:76 | ||||
| chr7:74027996-74028216 | Common:1; Rare:72; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 |