Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:209937982-209938262 | Common:3; Rare:96; Clinvar (pathogenic):1 | ||||
chr1:210232801-210232960 | Common:1; Rare:46 | ||||
chr1:211258968-211259413 | Common:3; Rare:156 | ||||
chr1:211259723-211259980 | Rare:73 | ||||
chr1:211675579-211675730 | Rare:34 | ||||
chr1:212035497-212035812 | Common:2; Rare:86 | ||||
chr1:212285066-212285440 | Common:3; Rare:122 | ||||
chr1:212285728-212286113 | Common:1; Rare:100 | ||||
chr1:212432792-212433117 | Rare:86 | ||||
chr1:212608290-212608377 | Common:2; Rare:21 | ||||
chr1:212608503-212608767 | Rare:65 | ||||
chr1:212615543-212615809 | Common:1; Rare:42 | ||||
chr1:212699703-212700069 | Common:6; Rare:96 | ||||
chr1:212791687-212791982 | Common:6; Rare:141 | ||||
chr1:212858070-212858303 | Common:4; Rare:61; Clinvar:2 |