Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:21002092-21002232 | Common:3; Rare:50 | ||||
chr22:23145171-23145515 | Common:3; Rare:109 | ||||
chr22:23696227-23696472 | Common:1; Rare:51 | ||||
chr22:23786923-23787025 | Common:1; Rare:44; Clinvar:3 | ||||
chr22:23857684-23857908 | Common:1; Rare:76 | ||||
chr22:23894311-23894502 | Common:3; Rare:69 | ||||
chr22:24555913-24556060 | Rare:42 | ||||
chr22:26483763-26484015 | Common:6; Rare:107; Clinvar:5; Clinvar (benign):1 | ||||
chr22:26512428-26512542 | Common:1; Rare:53 | ||||
chr22:26590112-26590220 | Common:2; Rare:47 | ||||
chr22:27919195-27919518 | Common:5; Rare:144 | ||||
chr22:28741798-28742090 | Common:2; Rare:91; Clinvar:1; Clinvar (benign):1 | ||||
chr22:28742397-28742701 | Common:1; Rare:73 | ||||
chr22:28800347-28800702 | Common:5; Rare:128 | ||||
chr22:29205785-29206031 | Common:1; Rare:69 |