| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:64563002-64563261 | Common:4; Rare:72 | ||||
| chr7:64665985-64666195 | Common:4; Rare:46 | ||||
| chr7:64794267-64794512 | Common:4; Rare:68 | ||||
| chr7:65373690-65373940 | Rare:80 | ||||
| chr7:65982156-65982322 | Common:3; Rare:58; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr7:66075574-66075963 | Rare:103; Clinvar (benign):1 | ||||
| chr7:66114765-66114963 | Common:1; Rare:90 | ||||
| chr7:66115238-66115357 | Rare:25 | ||||
| chr7:66628636-66629001 | Common:2; Rare:135; Clinvar:6 | ||||
| chr7:66681942-66682227 | Common:6; Rare:115 | ||||
| chr7:66921127-66921428 | Common:1; Rare:91 | ||||
| chr7:66996545-66996850 | Common:3; Rare:69 | ||||
| chr7:71132656-71132883 | Common:1; Rare:60 | ||||
| chr7:72337368-72337466 | Common:1; Rare:42 | ||||
| chr7:72828180-72828483 | Rare:75 |