Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:24187258-24187464 | Common:8; Rare:66 | ||||
chr1:24413697-24413855 | Common:1; Rare:36 | ||||
chr1:24642920-24643326 | Common:2; Rare:137 | ||||
chr1:25232442-25232596 | Rare:63 | ||||
chr1:25247449-25247630 | Common:2; Rare:63 | ||||
chr1:25338190-25338447 | Common:1; Rare:91 | ||||
chr1:25819885-25820013 | Common:2; Rare:38 | ||||
chr1:25859332-25859533 | Common:3; Rare:86 | ||||
chr1:25906392-25906601 | Rare:80 | ||||
chr1:26279953-26280162 | Rare:121 | ||||
chr1:26306623-26306860 | Common:13; Rare:73 | ||||
chr1:26432167-26432406 | Common:4; Rare:69; Clinvar:2; Clinvar (benign):1 | ||||
chr1:26890241-26890336 | Common:1; Rare:40 | ||||
chr1:27341802-27342092 | Rare:62 | ||||
chr1:27773110-27773269 | Rare:56 |