Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:38264256-38264691 | Common:6; Rare:107 | ||||
chr19:38618947-38619246 | Common:3; Rare:88 | ||||
chr19:38736953-38737112 | Common:3; Rare:17 | ||||
chr19:38812935-38813263 | Common:2; Rare:61 | ||||
chr19:38831755-38832061 | Common:4; Rare:93; Clinvar (benign):1 | ||||
chr19:38852319-38852608 | Rare:71 | ||||
chr19:38899572-38899959 | Rare:106 | ||||
chr19:38930742-38930992 | Common:3; Rare:65; Clinvar:2; Clinvar (benign):3 | ||||
chr19:39203864-39203955 | Common:1; Rare:36 | ||||
chr19:39203965-39204312 | Common:1; Rare:135 | ||||
chr19:39391045-39391435 | Common:1; Rare:162 | ||||
chr19:39406689-39406866 | Rare:64 | ||||
chr19:39435854-39436165 | Common:7; Rare:113 | ||||
chr19:39846301-39846520 | Common:1; Rare:108 | ||||
chr19:39970954-39971200 | Common:3; Rare:65 |