| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:50450306-50450467 | Common:1; Rare:71 | ||||
| chr7:55365943-55366073 | Rare:55 | ||||
| chr7:55366273-55366392 | Common:1; Rare:45 | ||||
| chr7:55572341-55572561 | Common:1; Rare:92 | ||||
| chr7:56051380-56051983 | Common:1; Rare:211; Clinvar:5; Clinvar (benign):1 | ||||
| chr7:56064215-56064372 | Common:1; Rare:107 | ||||
| chr7:56106392-56106681 | Common:8; Rare:103 | ||||
| chr7:64563015-64563261 | Common:4; Rare:66 | ||||
| chr7:64794277-64794463 | Common:4; Rare:51 | ||||
| chr7:65006660-65006866 | Common:2; Rare:57 | ||||
| chr7:65982156-65982311 | Common:3; Rare:55; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr7:66114752-66114960 | Common:1; Rare:93 | ||||
| chr7:66115169-66115374 | Common:1; Rare:47 | ||||
| chr7:66628629-66629001 | Common:2; Rare:138; Clinvar:6 | ||||
| chr7:66681972-66682207 | Common:6; Rare:102 |