Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:32464963-32465098 | Rare:41 | ||||
chr1:32539399-32539529 | Rare:32 | ||||
chr1:32650489-32650657 | Common:1; Rare:77 | ||||
chr1:32650881-32651328 | Common:2; Rare:161 | ||||
chr1:32651626-32652060 | Common:2; Rare:99 | ||||
chr1:32702625-32702888 | Rare:68 | ||||
chr1:32753872-32754037 | Common:1; Rare:58 | ||||
chr1:32765679-32765799 | Common:2; Rare:31 | ||||
chr1:32817233-32817844 | Common:1; Rare:160; Clinvar:5; Clinvar (benign):4 | ||||
chr1:32897765-32897911 | Rare:23 | ||||
chr1:33036826-33037121 | Rare:104; Clinvar (pathogenic):1 | ||||
chr1:33080956-33081194 | Common:2; Rare:69 | ||||
chr1:33430997-33431248 | Common:2; Rare:69 | ||||
chr1:33472548-33472691 | Rare:28 | ||||
chr1:34177259-34177590 | Common:1; Rare:67 |