Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:161118012-161118146 | Rare:68 | ||||
chr1:161132426-161132855 | Common:2; Rare:138 | ||||
chr1:161166268-161166499 | Common:2; Rare:56; Clinvar:2; Clinvar (benign):1 | ||||
chr1:161197156-161197428 | Common:3; Rare:43 | ||||
chr1:161199010-161199326 | Rare:47 | ||||
chr1:161314262-161314423 | Common:3; Rare:65; Clinvar:9; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr1:161766147-161766376 | Common:3; Rare:69 | ||||
chr1:162023635-162023934 | Common:1; Rare:82 | ||||
chr1:162561346-162561700 | Common:3; Rare:134 | ||||
chr1:162631326-162631394 | Rare:10 | ||||
chr1:162632129-162632624 | Rare:84 | ||||
chr1:162790573-162790781 | Common:4; Rare:60 | ||||
chr1:163202795-163203221 | Common:1; Rare:84 | ||||
chr1:163321683-163322047 | Common:1; Rare:101 | ||||
chr1:165630854-165631181 | Common:4; Rare:84 |