Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:161153710-161153836 | Rare:31 | ||||
chr1:161159340-161159541 | Common:2; Rare:61 | ||||
chr1:161166268-161166512 | Common:2; Rare:60; Clinvar:3; Clinvar (benign):1 | ||||
chr1:161225745-161226078 | Common:10; Rare:49 | ||||
chr1:161258495-161258822 | Common:2; Rare:81 | ||||
chr1:161314238-161314443 | Common:4; Rare:81; Clinvar:10; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
chr1:161749632-161749885 | Rare:91 | ||||
chr1:161750214-161750488 | Rare:56 | ||||
chr1:161766213-161766529 | Common:5; Rare:100; Clinvar (pathogenic):1 | ||||
chr1:162497756-162497874 | Common:2; Rare:43 | ||||
chr1:162561351-162561573 | Common:3; Rare:93 | ||||
chr1:162790516-162790809 | Common:4; Rare:86 | ||||
chr1:163321695-163322007 | Common:1; Rare:82 | ||||
chr1:164559301-164559529 | Rare:59 | ||||
chr1:164559572-164559785 | Common:2; Rare:49 |