Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:20507473-20507622 | Rare:41 | ||||
chr22:21002043-21002187 | Common:3; Rare:56 | ||||
chr22:21938138-21938295 | Rare:58 | ||||
chr22:23894295-23894480 | Common:3; Rare:65 | ||||
chr22:24011065-24011335 | Common:42; Rare:157 | ||||
chr22:24555873-24556066 | Rare:57 | ||||
chr22:26483775-26484010 | Common:6; Rare:97; Clinvar:5; Clinvar (benign):1 | ||||
chr22:26512428-26512555 | Common:1; Rare:56 | ||||
chr22:27919190-27919510 | Common:5; Rare:142 | ||||
chr22:28741789-28742087 | Common:2; Rare:95; Clinvar:1; Clinvar (benign):3 | ||||
chr22:28800426-28800702 | Common:5; Rare:106 | ||||
chr22:29205751-29206052 | Common:1; Rare:79 | ||||
chr22:29267950-29268339 | Common:2; Rare:115 | ||||
chr22:29766963-29767432 | Common:4; Rare:137 | ||||
chr22:30356855-30356983 | Common:1; Rare:46 |