Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:161258565-161258747 | Common:1; Rare:33 | ||||
chr1:161314251-161314469 | Common:4; Rare:88; Clinvar:10; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
chr1:161749608-161750060 | Rare:163 | ||||
chr1:161750207-161750429 | Rare:53 | ||||
chr1:161766140-161766364 | Common:3; Rare:64 | ||||
chr1:162023636-162024008 | Common:1; Rare:112 | ||||
chr1:162069440-162069790 | Common:1; Rare:87 | ||||
chr1:162497710-162497908 | Common:3; Rare:65 | ||||
chr1:162561259-162561745 | Common:5; Rare:179 | ||||
chr1:162790499-162790787 | Common:4; Rare:81 | ||||
chr1:163069238-163069375 | Rare:43 | ||||
chr1:163202911-163203595 | Common:3; Rare:145 | ||||
chr1:163321670-163322026 | Common:1; Rare:97 | ||||
chr1:164558782-164559235 | Common:1; Rare:116 | ||||
chr1:164559279-164559506 | Rare:57 |