Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:161199049-161199332 | Rare:45 | ||||
chr1:161225741-161226069 | Common:10; Rare:49 | ||||
chr1:161314262-161314397 | Common:3; Rare:47; Clinvar (benign):2 | ||||
chr1:161706942-161707273 | Common:3; Rare:71 | ||||
chr1:161749703-161749859 | Rare:58 | ||||
chr1:161766133-161766363 | Common:3; Rare:67 | ||||
chr1:162023630-162024027 | Common:1; Rare:123 | ||||
chr1:162497707-162497867 | Common:2; Rare:51 | ||||
chr1:163321723-163322105 | Common:1; Rare:102 | ||||
chr1:165698504-165698757 | Common:5; Rare:98 | ||||
chr1:165768765-165769039 | Common:2; Rare:111 | ||||
chr1:167093985-167094084 | Rare:19 | ||||
chr1:167935952-167936261 | Common:1; Rare:94 | ||||
chr1:167936528-167936985 | Common:1; Rare:166 | ||||
chr1:168178662-168179074 | Common:4; Rare:123 |