Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:44222083-44222248 | Rare:35 | ||||
chr17:44503377-44503527 | Rare:59 | ||||
chr17:44899369-44899741 | Common:2; Rare:116; Clinvar:2; Clinvar (benign):1 | ||||
chr17:45061104-45061351 | Common:1; Rare:75 | ||||
chr17:46922858-46923182 | Common:4; Rare:87; Clinvar (benign):7 | ||||
chr17:47189235-47189619 | Rare:98 | ||||
chr17:47323890-47323962 | Rare:21 | ||||
chr17:47831515-47831597 | Rare:26 | ||||
chr17:47941352-47941719 | Rare:101; Clinvar:6; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
chr17:48048039-48048379 | Common:1; Rare:91 | ||||
chr17:48723004-48723206 | Rare:44 | ||||
chr17:48729015-48729198 | Rare:37 | ||||
chr17:48944758-48944918 | Common:2; Rare:56 | ||||
chr17:49414833-49415140 | Common:2; Rare:74 | ||||
chr17:49788361-49788708 | Common:1; Rare:101 |