Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:43515133-43515275 | Common:3; Rare:52 | ||||
chr5:43602411-43602741 | Common:2; Rare:55 | ||||
chr5:43602852-43603266 | Rare:100 | ||||
chr5:44808727-44808959 | Common:2; Rare:77 | ||||
chr5:52989185-52989365 | Common:4; Rare:53; Clinvar (benign):1 | ||||
chr5:53109701-53109903 | Common:1; Rare:103; Clinvar:5; Clinvar (pathogenic):1 | ||||
chr5:54310513-54310711 | Rare:63 | ||||
chr5:55307627-55308016 | Common:4; Rare:132 | ||||
chr5:57173768-57174118 | Common:1; Rare:117 | ||||
chr5:58460019-58460206 | Common:5; Rare:78 | ||||
chr5:59039775-59039991 | Common:2; Rare:61 | ||||
chr5:60700129-60700237 | Common:1; Rare:32 | ||||
chr5:60945038-60945245 | Common:4; Rare:78; Clinvar:2; Clinvar (benign):4 | ||||
chr5:61162328-61162558 | Common:1; Rare:58 | ||||
chr5:62403859-62404042 | Common:3; Rare:60 |