Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:161153750-161154073 | Common:1; Rare:97; Clinvar (pathogenic):1 | ||||
chr1:161166268-161166477 | Common:2; Rare:49; Clinvar:2; Clinvar (benign):1 | ||||
chr1:161198950-161199326 | Rare:58 | ||||
chr1:161215133-161215331 | Common:2; Rare:57 | ||||
chr1:161225768-161226094 | Common:10; Rare:49 | ||||
chr1:161314318-161314412 | Common:2; Rare:39; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr1:161505188-161505510 | Common:1; Rare:65 | ||||
chr1:162023611-162023915 | Common:1; Rare:84 | ||||
chr1:162497726-162497864 | Common:2; Rare:43 | ||||
chr1:162561365-162561750 | Common:4; Rare:139 | ||||
chr1:162632256-162632563 | Rare:60 | ||||
chr1:163069070-163069478 | Rare:108 | ||||
chr1:163203046-163203271 | Common:1; Rare:44 | ||||
chr1:163321723-163322057 | Common:1; Rare:91 | ||||
chr1:165768768-165769019 | Common:2; Rare:104 |