Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:122879518-122879681 | Common:3; Rare:46 | ||||
chr10:122954171-122954434 | Rare:90 | ||||
chr10:123008722-123009023 | Common:6; Rare:80; Clinvar:4; Clinvar (benign):5 | ||||
chr10:124791819-124791938 | Rare:57 | ||||
chr10:125823176-125823645 | Common:2; Rare:169; Clinvar:1; Clinvar (benign):2 | ||||
chr10:126388236-126388508 | Common:1; Rare:86 | ||||
chr10:126905292-126905456 | Rare:63 | ||||
chr10:131981886-131982143 | Common:2; Rare:94 | ||||
chr10:132307876-132308137 | Common:3; Rare:81 | ||||
chr10:132331813-132332116 | Common:12; Rare:98 | ||||
chr10:133308835-133308982 | Rare:69 | ||||
chr11:207322-207732 | Common:8; Rare:138 | ||||
chr11:208633-208852 | Rare:81 | ||||
chr11:236919-237028 | Rare:40 | ||||
chr11:308077-308319 | Common:5; Rare:78 |