Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:121927899-121928195 | Common:2; Rare:90 | ||||
chr10:121928421-121928528 | Rare:33 | ||||
chr10:122879525-122879717 | Common:3; Rare:51 | ||||
chr10:122954179-122954515 | Common:1; Rare:122 | ||||
chr10:123008722-123009044 | Common:6; Rare:92; Clinvar:4; Clinvar (benign):5 | ||||
chr10:125158715-125158866 | Rare:44 | ||||
chr10:125719456-125719734 | Common:1; Rare:88 | ||||
chr10:125823030-125823708 | Common:3; Rare:229; Clinvar:2; Clinvar (benign):3 | ||||
chr10:125896462-125896600 | Common:1; Rare:7 | ||||
chr10:126905332-126905479 | Rare:56 | ||||
chr10:131981889-131982143 | Common:2; Rare:93 | ||||
chr10:132331819-132332190 | Common:13; Rare:113 | ||||
chr10:133308829-133308968 | Rare:66 | ||||
chr10:133309126-133309402 | Common:2; Rare:97 | ||||
chr11:207327-207726 | Common:8; Rare:134 |