Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:186375669-186375928 | Common:1; Rare:68 | ||||
chr1:186680343-186680627 | Common:3; Rare:63 | ||||
chr1:190477526-190477721 | Common:2; Rare:50 | ||||
chr1:190477853-190478548 | Common:2; Rare:151 | ||||
chr1:190478666-190478993 | Common:6; Rare:84 | ||||
chr1:193059280-193059673 | Rare:189 | ||||
chr1:193105384-193105515 | Common:1; Rare:53 | ||||
chr1:193121650-193122216 | Common:3; Rare:198; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr1:193186532-193186728 | Rare:36 | ||||
chr1:197268118-197268308 | Rare:33; Clinvar:1; Clinvar (benign):1 | ||||
chr1:200410005-200410234 | Rare:68 | ||||
chr1:200669861-200670045 | Common:11; Rare:73 | ||||
chr1:201154438-201154658 | Common:2; Rare:59 | ||||
chr1:201648016-201648201 | Rare:37 | ||||
chr1:201829054-201829205 | Rare:70 |