Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:161166268-161166511 | Common:2; Rare:59; Clinvar:3; Clinvar (benign):1 | ||||
chr1:161199046-161199329 | Rare:45 | ||||
chr1:161215092-161215330 | Common:2; Rare:63 | ||||
chr1:161314264-161314416 | Common:3; Rare:59; Clinvar:6; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr1:161766252-161766376 | Common:1; Rare:44 | ||||
chr1:162561351-162561730 | Common:4; Rare:146 | ||||
chr1:162632254-162632624 | Rare:68 | ||||
chr1:163202795-163203082 | Rare:56 | ||||
chr1:163321723-163322007 | Common:1; Rare:76 | ||||
chr1:164559596-164559780 | Common:2; Rare:41 | ||||
chr1:165698466-165698759 | Common:5; Rare:120 | ||||
chr1:165768719-165768926 | Common:1; Rare:81; Clinvar:1 | ||||
chr1:166839243-166839539 | Rare:90 | ||||
chr1:167721773-167722038 | Common:4; Rare:73 | ||||
chr1:167935931-167936329 | Common:2; Rare:117 |