Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:44808727-44808959 | Common:2; Rare:77 | ||||
chr5:50666904-50666967 | Rare:21 | ||||
chr5:52787877-52788247 | Common:1; Rare:76 | ||||
chr5:53109725-53109906 | Common:1; Rare:91; Clinvar:2 | ||||
chr5:53482048-53482195 | Rare:36 | ||||
chr5:55307620-55308056 | Common:5; Rare:157 | ||||
chr5:55952009-55952296 | Common:1; Rare:62 | ||||
chr5:56952098-56952471 | Rare:128 | ||||
chr5:60944968-60945238 | Common:5; Rare:109; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr5:61162243-61162507 | Common:1; Rare:57 | ||||
chr5:62403791-62404032 | Common:3; Rare:90 | ||||
chr5:64768538-64769039 | Common:5; Rare:128 | ||||
chr5:65481574-65481668 | Rare:22 | ||||
chr5:65481793-65482065 | Common:1; Rare:50 | ||||
chr5:65563092-65563323 | Common:4; Rare:85 |