Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:161166268-161166516 | Common:2; Rare:60; Clinvar:3; Clinvar (benign):1 | ||||
chr1:161199051-161199326 | Rare:43 | ||||
chr1:161223611-161223921 | Common:1; Rare:55; Clinvar:1 | ||||
chr1:161225768-161226082 | Common:10; Rare:45 | ||||
chr1:161314292-161314417 | Common:2; Rare:52; Clinvar:7; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr1:161766163-161766385 | Common:3; Rare:72 | ||||
chr1:162023638-162023675 | Rare:11 | ||||
chr1:162497751-162497859 | Common:1; Rare:34 | ||||
chr1:162632129-162632563 | Rare:76 | ||||
chr1:162790542-162790777 | Common:4; Rare:66 | ||||
chr1:163202853-163203199 | Common:1; Rare:68 | ||||
chr1:163321703-163322077 | Common:1; Rare:99 | ||||
chr1:165698461-165698711 | Common:3; Rare:113 | ||||
chr1:165768696-165769040 | Common:2; Rare:126; Clinvar:1 | ||||
chr1:166839322-166839550 | Rare:64 |