Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:17628649-17628860 | Common:2; Rare:73 | ||||
chr22:19447684-19447914 | Common:2; Rare:88 | ||||
chr22:19854782-19854972 | Common:1; Rare:65 | ||||
chr22:19941744-19942129 | Common:2; Rare:101; Clinvar:4 | ||||
chr22:20117090-20117612 | Common:3; Rare:162 | ||||
chr22:20437808-20438006 | Rare:52 | ||||
chr22:20495775-20496002 | Common:2; Rare:83 | ||||
chr22:20858736-20859096 | Common:5; Rare:182; Clinvar:3; Clinvar (benign):3 | ||||
chr22:21002092-21002151 | Common:3; Rare:20 | ||||
chr22:21867610-21867840 | Common:2; Rare:76 | ||||
chr22:23894331-23894475 | Common:3; Rare:51 | ||||
chr22:23894570-23894814 | Common:3; Rare:95 | ||||
chr22:24555030-24555485 | Common:4; Rare:165 | ||||
chr22:24555830-24556030 | Rare:64 | ||||
chr22:26483786-26483909 | Common:4; Rare:46; Clinvar:4; Clinvar (benign):1 |