Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:124791756-124791941 | Common:1; Rare:97 | ||||
chr10:125719453-125719795 | Common:1; Rare:129 | ||||
chr10:125823200-125823611 | Common:1; Rare:144; Clinvar:1; Clinvar (benign):1 | ||||
chr10:125896233-125896628 | Common:5; Rare:31 | ||||
chr10:126905297-126905473 | Rare:69 | ||||
chr10:128047382-128047664 | Common:4; Rare:99 | ||||
chr10:131981792-131982134 | Common:4; Rare:119 | ||||
chr10:132331813-132332216 | Common:14; Rare:131 | ||||
chr10:133308829-133308982 | Rare:72 | ||||
chr10:133527009-133527368 | Common:6; Rare:55 | ||||
chr10:133527956-133528105 | Rare:45 | ||||
chr10:133528392-133528501 | Common:2; Rare:41 | ||||
chr11:207331-207740 | Common:9; Rare:140 | ||||
chr11:208662-208865 | Rare:79 | ||||
chr11:236324-236525 | Common:6; Rare:66 |