Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:23894054-23894555 | Common:5; Rare:150 | ||||
chr22:23894578-23894903 | Common:3; Rare:130; Clinvar:1 | ||||
chr22:24270607-24270940 | Common:4; Rare:120 | ||||
chr22:24270947-24271174 | Common:2; Rare:86 | ||||
chr22:24555035-24555430 | Common:4; Rare:138 | ||||
chr22:24555880-24556035 | Rare:49 | ||||
chr22:26483736-26483883 | Common:4; Rare:62; Clinvar:6; Clinvar (benign):1 | ||||
chr22:26512428-26512552 | Common:1; Rare:55 | ||||
chr22:26565229-26565447 | Rare:38 | ||||
chr22:26590077-26590220 | Common:3; Rare:58 | ||||
chr22:27919195-27919510 | Common:5; Rare:139 | ||||
chr22:28741804-28742078 | Common:2; Rare:80; Clinvar:1 | ||||
chr22:28800301-28800781 | Common:7; Rare:167 | ||||
chr22:29205762-29206039 | Common:1; Rare:75 | ||||
chr22:29267894-29268348 | Common:2; Rare:130 |