Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr21:44299958-44300078 | Common:1; Rare:44 | ||||
chr21:45981500-45981813 | Common:23; Rare:71; Clinvar (benign):2 | ||||
chr22:17628737-17629084 | Common:3; Rare:100 | ||||
chr22:24555892-24556050 | Rare:49 | ||||
chr22:26512428-26512550 | Common:1; Rare:55 | ||||
chr22:29267950-29268329 | Common:2; Rare:110 | ||||
chr22:29767053-29767416 | Common:4; Rare:117 | ||||
chr22:31081175-31081328 | Common:1; Rare:36 | ||||
chr22:37849331-37849443 | Rare:62 | ||||
chr22:38656382-38656678 | Common:1; Rare:70 | ||||
chr22:38681908-38681979 | Rare:33 | ||||
chr22:41621000-41621360 | Common:7; Rare:134 | ||||
chr22:41832921-41833133 | Common:3; Rare:66 | ||||
chr22:42090737-42090945 | Common:1; Rare:72; Clinvar (pathogenic):1 | ||||
chr22:50783639-50783859 | Common:1; Rare:62 |