Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:24187258-24187464 | Not yet | Common:8; Rare:66 | 229 | ||
chr1:24413697-24413855 | Not yet | Common:1; Rare:36 | 263 | ||
chr1:24642920-24643326 | Not yet | Common:2; Rare:137 | 308 | ||
chr1:25232442-25232596 | Not yet | Rare:63 | 227 | ||
chr1:25247449-25247630 | Not yet | Common:2; Rare:63 | 177 | ||
chr1:25338190-25338447 | Not yet | Common:1; Rare:91 | 261 | ||
chr1:25819885-25820013 | Not yet | Common:2; Rare:38 | 175 | ||
chr1:25859332-25859533 | Not yet | Common:3; Rare:86 | 164 | ||
chr1:25906392-25906601 | Not yet | Rare:80 | 235 | ||
chr1:26279953-26280162 | Not yet | Rare:121 | 259 | ||
chr1:26306623-26306860 | Not yet | Common:13; Rare:73 | 275 | ||
chr1:26432167-26432406 | Not yet | Common:4; Rare:69; Clinvar:2; Clinvar (benign):1 | 337 | ||
chr1:26890241-26890336 | Not yet | Common:1; Rare:40 | 155 | ||
chr1:27341802-27342092 | Not yet | Rare:62 | 285 | ||
chr1:27773110-27773269 | Not yet | Rare:56 | 178 |