Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:161399597-161399855 | Common:6; Rare:157 | ||||
chr1:161810526-161810600 | Rare:12 | ||||
chr1:161820945-161821168 | Rare:57; Clinvar (pathogenic):2 | ||||
chr1:161821716-161821788 | Rare:10 | ||||
chr1:162458256-162458262 | |||||
chr1:162479316-162479503 | Common:2; Rare:45 | ||||
chr1:162571337-162571542 | Common:2; Rare:34 | ||||
chr1:162633265-162633564 | Common:1; Rare:66 | ||||
chr1:162984813-162984945 | Rare:25 | ||||
chr1:163328055-163328318 | Common:1; Rare:50 | ||||
chr1:163993077-163993094 | Rare:3 | ||||
chr1:165651926-165652035 | Rare:30 | ||||
chr1:165676198-165676494 | Common:1; Rare:53 | ||||
chr1:165896943-165897184 | Rare:48 | ||||
chr1:167266712-167266815 | Common:1; Rare:9 |