Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:122954197-122954464 | Rare:98 | ||||
chr10:123008788-123009028 | Common:5; Rare:66; Clinvar:4; Clinvar (benign):5 | ||||
chr10:125719468-125719755 | Common:1; Rare:104 | ||||
chr10:125823185-125823594 | Common:2; Rare:147; Clinvar:1; Clinvar (benign):2 | ||||
chr10:125896282-125896628 | Common:5; Rare:29 | ||||
chr10:129466974-129467283 | Common:4; Rare:119; Clinvar:1 | ||||
chr10:131981897-131982154 | Common:1; Rare:95 | ||||
chr10:132331876-132332155 | Common:12; Rare:66 | ||||
chr10:133308828-133308980 | Rare:71 | ||||
chr11:207372-207719 | Common:7; Rare:102 | ||||
chr11:208741-208852 | Rare:46 | ||||
chr11:236333-236503 | Common:6; Rare:50 | ||||
chr11:236917-237052 | Common:1; Rare:53 | ||||
chr11:506607-506629 | Rare:8 | ||||
chr11:506732-507001 | Common:3; Rare:92 |