| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:55572296-55572609 | Common:1; Rare:115 | ||||
| chr7:55887511-55887673 | Common:4; Rare:60 | ||||
| chr7:56051396-56051863 | Common:1; Rare:177; Clinvar:5; Clinvar (benign):1 | ||||
| chr7:56064177-56064372 | Common:2; Rare:121 | ||||
| chr7:56106362-56106682 | Common:8; Rare:118 | ||||
| chr7:64562970-64563262 | Common:5; Rare:85 | ||||
| chr7:64794277-64794495 | Common:4; Rare:61 | ||||
| chr7:65006578-65006866 | Common:2; Rare:84 | ||||
| chr7:66075574-66075954 | Rare:102; Clinvar (benign):1 | ||||
| chr7:66114732-66114965 | Common:2; Rare:99 | ||||
| chr7:66115177-66115354 | Common:1; Rare:41 | ||||
| chr7:66628682-66628990 | Common:2; Rare:113; Clinvar:5 | ||||
| chr7:66682005-66682192 | Common:6; Rare:91 | ||||
| chr7:66921130-66921469 | Common:1; Rare:101 | ||||
| chr7:66995394-66995711 | Rare:94; Clinvar (pathogenic):1 |