Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:41446553-41446651 | Common:2; Rare:30 | ||||
chr22:41446778-41446948 | Rare:66 | ||||
chr22:41468657-41468759 | Common:2; Rare:31 | ||||
chr22:41469063-41469149 | Rare:35 | ||||
chr22:41560904-41561068 | Common:2; Rare:43 | ||||
chr22:41621006-41621384 | Common:7; Rare:137 | ||||
chr22:41800506-41800679 | Rare:55 | ||||
chr22:41832909-41833291 | Common:3; Rare:137 | ||||
chr22:42070770-42070959 | Common:2; Rare:41 | ||||
chr22:42079632-42079738 | Common:1; Rare:29 | ||||
chr22:42090607-42091001 | Common:2; Rare:167; Clinvar (pathogenic):1 | ||||
chr22:42614937-42615251 | Common:3; Rare:132 | ||||
chr22:42649327-42649452 | Rare:56 | ||||
chr22:42857177-42857445 | Common:3; Rare:112 | ||||
chr22:43143374-43143470 | Common:2; Rare:27 |