Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:37849316-37849468 | Rare:85 | ||||
chr22:37906140-37906339 | Common:1; Rare:54 | ||||
chr22:37953591-37953767 | Rare:76 | ||||
chr22:38656363-38656732 | Common:1; Rare:96 | ||||
chr22:38681821-38682091 | Common:2; Rare:109 | ||||
chr22:39319604-39319832 | Common:2; Rare:93 | ||||
chr22:41286161-41286424 | Common:2; Rare:81 | ||||
chr22:41469016-41469170 | Rare:62 | ||||
chr22:41621026-41621380 | Common:7; Rare:131 | ||||
chr22:41947084-41947189 | Common:1; Rare:39 | ||||
chr22:42090735-42090931 | Common:1; Rare:71; Clinvar (pathogenic):1 | ||||
chr22:42614901-42615244 | Common:3; Rare:132 | ||||
chr22:42649326-42649592 | Common:6; Rare:94 | ||||
chr22:43955270-43955554 | Common:3; Rare:83 | ||||
chr22:46250262-46250396 | Common:2; Rare:39 |