| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:55572341-55572631 | Common:1; Rare:106 | ||||
| chr7:55887500-55887673 | Common:4; Rare:64 | ||||
| chr7:55951739-55951942 | Rare:59 | ||||
| chr7:55964427-55964631 | Rare:70 | ||||
| chr7:56051384-56051851 | Common:1; Rare:176; Clinvar:5; Clinvar (benign):1 | ||||
| chr7:56064177-56064356 | Common:2; Rare:111 | ||||
| chr7:56106378-56106671 | Common:8; Rare:110 | ||||
| chr7:64562992-64563261 | Common:4; Rare:78 | ||||
| chr7:64794225-64794471 | Common:4; Rare:72 | ||||
| chr7:65006624-65006866 | Common:2; Rare:74 | ||||
| chr7:65982124-65982342 | Common:3; Rare:72; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr7:66114750-66114895 | Common:1; Rare:70 | ||||
| chr7:66115194-66115354 | Rare:35 | ||||
| chr7:66628640-66629026 | Common:3; Rare:143; Clinvar:7; Clinvar (benign):2 | ||||
| chr7:66682000-66682219 | Common:6; Rare:103 |