Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:18152990-18153292 | Common:1; Rare:100 | ||||
chr19:18557741-18557911 | Common:3; Rare:47 | ||||
chr19:18571629-18571906 | Common:4; Rare:114 | ||||
chr19:18683471-18683694 | Common:2; Rare:70 | ||||
chr19:18919344-18919738 | Common:2; Rare:137 | ||||
chr19:19033462-19033653 | Common:2; Rare:65 | ||||
chr19:19033805-19033882 | Rare:20 | ||||
chr19:19192113-19192268 | Common:1; Rare:50 | ||||
chr19:19192624-19192978 | Common:2; Rare:83 | ||||
chr19:19320485-19320870 | Common:4; Rare:138 | ||||
chr19:19516157-19516331 | Rare:103; Clinvar:1; Clinvar (pathogenic):1 | ||||
chr19:19668651-19668805 | Rare:33 | ||||
chr19:19821668-19821873 | Common:1; Rare:69 | ||||
chr19:21396925-21397173 | Rare:68 | ||||
chr19:21836126-21836331 | Rare:76 |