Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:23145468-23145515 | Common:1; Rare:19 | ||||
chr22:23750972-23751180 | Common:1; Rare:73 | ||||
chr22:23894137-23894492 | Common:5; Rare:113 | ||||
chr22:24245071-24245239 | Common:2; Rare:26 | ||||
chr22:24270595-24270915 | Common:4; Rare:116 | ||||
chr22:24555880-24556071 | Rare:56 | ||||
chr22:24952608-24952753 | Rare:42 | ||||
chr22:26483768-26483949 | Common:4; Rare:69; Clinvar:5; Clinvar (benign):1 | ||||
chr22:26512428-26512552 | Common:1; Rare:55 | ||||
chr22:26590085-26590223 | Common:3; Rare:54 | ||||
chr22:27919175-27919538 | Common:5; Rare:161 | ||||
chr22:28712465-28712650 | Common:1; Rare:24 | ||||
chr22:28741806-28742103 | Common:2; Rare:90 | ||||
chr22:28742408-28742701 | Common:1; Rare:73 | ||||
chr22:28800554-28800709 | Common:2; Rare:50 |