Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:233613990-233614377 | Common:5; Rare:147 | ||||
chr1:234373302-234373792 | Common:1; Rare:215; Clinvar (benign):7 | ||||
chr1:234608173-234608293 | Rare:39 | ||||
chr1:235128764-235129048 | Rare:116 | ||||
chr1:235328109-235328636 | Common:4; Rare:164 | ||||
chr1:235328791-235329018 | Common:1; Rare:75 | ||||
chr1:236064991-236065344 | Common:2; Rare:129; Clinvar (pathogenic):1 | ||||
chr1:236523861-236524060 | Common:2; Rare:51 | ||||
chr1:236540478-236540672 | Common:3; Rare:66 | ||||
chr1:236604456-236604624 | Common:4; Rare:53 | ||||
chr1:239386502-239386676 | Rare:23 | ||||
chr1:241848108-241848255 | Common:1; Rare:26 | ||||
chr1:243255047-243255358 | Common:1; Rare:69 | ||||
chr1:243255770-243256157 | Common:1; Rare:116; Clinvar:4; Clinvar (benign):1 | ||||
chr1:243487456-243487852 | Common:5; Rare:91 |