Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr9:134644700-134644899 | Common:1; Rare:34 | ||||
chr9:134750555-134750820 | Common:5; Rare:72; Clinvar:6; Clinvar (benign):8 | ||||
chr9:134800785-134800961 | Common:2; Rare:28 | ||||
chr9:134825859-134826164 | Common:3; Rare:79; Clinvar:4; Clinvar (benign):3 | ||||
chr9:134826221-134826433 | Common:5; Rare:33 | ||||
chr9:134833735-134833983 | Rare:45 | ||||
chr9:135995270-135995420 | Common:1; Rare:39 | ||||
chr9:136376479-136376524 | Common:1; Rare:10 | ||||
chr9:136400139-136400328 | Common:2; Rare:64 | ||||
chr9:136438939-136439066 | Rare:45; Clinvar (pathogenic):1 | ||||
chr9:136447853-136448103 | Rare:53 | ||||
chr9:136724722-136725041 | Common:5; Rare:72 | ||||
chr9:136725745-136725784 | Rare:12 | ||||
chr9:136728159-136728354 | Common:3; Rare:82 | ||||
chr9:136839435-136839847 | Common:1; Rare:156 |