Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:122954197-122954484 | Rare:106 | ||||
chr10:123008788-123009011 | Common:5; Rare:60; Clinvar:4; Clinvar (benign):5 | ||||
chr10:124791813-124791938 | Rare:61 | ||||
chr10:125719464-125719739 | Common:1; Rare:92 | ||||
chr10:125823200-125823568 | Common:1; Rare:121; Clinvar:1; Clinvar (benign):1 | ||||
chr10:125896450-125896589 | Common:1; Rare:6 | ||||
chr10:126905268-126905460 | Rare:75 | ||||
chr10:131981796-131982160 | Common:4; Rare:129 | ||||
chr10:132331795-132332183 | Common:16; Rare:124 | ||||
chr10:133308835-133308974 | Rare:66 | ||||
chr11:207332-207736 | Common:8; Rare:137 | ||||
chr11:208615-208844 | Rare:80 | ||||
chr11:236720-237049 | Common:4; Rare:105 | ||||
chr11:307579-307792 | Common:6; Rare:61 | ||||
chr11:308004-308445 | Common:15; Rare:140 |