Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:218345227-218345349 | Rare:22 | ||||
chr1:220879990-220880043 | Rare:16 | ||||
chr1:220880075-220880153 | Rare:26 | ||||
chr1:220880169-220880253 | Common:2; Rare:27 | ||||
chr1:223992554-223992789 | Common:4; Rare:87 | ||||
chr1:226939127-226939466 | Common:4; Rare:52 | ||||
chr1:228276017-228276119 | Common:1; Rare:32 | ||||
chr1:228735726-228735899 | Rare:44 | ||||
chr1:229563755-229563922 | Common:2; Rare:20 | ||||
chr1:234531084-234531342 | Common:1; Rare:37 | ||||
chr1:234600055-234600265 | Common:7; Rare:93 | ||||
chr1:234610154-234610320 | Common:2; Rare:70 | ||||
chr1:236067011-236067296 | Common:2; Rare:49 | ||||
chr1:244451144-244451252 | Common:2; Rare:29 | ||||
chr1:244863721-244863959 | Rare:80; Clinvar:4; Clinvar (benign):4 |