Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:125896316-125896583 | Common:2; Rare:13 | ||||
chr10:126905302-126905460 | Rare:61 | ||||
chr10:131981865-131982155 | Common:4; Rare:108 | ||||
chr10:132186741-132186919 | Common:9; Rare:44 | ||||
chr10:132331816-132332229 | Common:13; Rare:133 | ||||
chr10:133308835-133308984 | Rare:70 | ||||
chr10:133336861-133337046 | Rare:68 | ||||
chr10:133373331-133373747 | Common:2; Rare:164; Clinvar (benign):1 | ||||
chr10:133393988-133394263 | Common:2; Rare:125 | ||||
chr10:133528022-133528105 | Rare:27 | ||||
chr11:207381-207740 | Common:8; Rare:107 | ||||
chr11:208688-208857 | Rare:69 | ||||
chr11:236331-236491 | Common:6; Rare:46 | ||||
chr11:236871-237071 | Common:1; Rare:76 | ||||
chr11:506732-507007 | Common:3; Rare:94 |