Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:43603054-43603288 | Rare:58 | ||||
chr5:44808765-44808976 | Common:2; Rare:68 | ||||
chr5:53109705-53109870 | Common:1; Rare:86; Clinvar:4; Clinvar (pathogenic):1 | ||||
chr5:54310507-54310714 | Rare:67 | ||||
chr5:54455583-54456105 | Common:2; Rare:164; Clinvar:6; Clinvar (benign):6 | ||||
chr5:55160067-55160205 | Rare:31 | ||||
chr5:55307611-55308106 | Common:5; Rare:186 | ||||
chr5:55534949-55535229 | Common:1; Rare:95 | ||||
chr5:55994784-55995148 | Common:1; Rare:116 | ||||
chr5:56952098-56952304 | Rare:74 | ||||
chr5:57173540-57173888 | Common:3; Rare:129 | ||||
chr5:58460053-58460192 | Common:3; Rare:57 | ||||
chr5:59039158-59039199 | Rare:7 | ||||
chr5:60700129-60700224 | Common:1; Rare:29 | ||||
chr5:60945009-60945382 | Common:6; Rare:150; Clinvar:7; Clinvar (benign):7; Clinvar (pathogenic):2 |