Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:11089295-11089559 | Rare:55; Clinvar:13; Clinvar (pathogenic):1 | ||||
chr19:11155689-11156016 | Common:2; Rare:91 | ||||
chr19:11197504-11197622 | Common:1; Rare:32 | ||||
chr19:11446861-11447137 | Common:2; Rare:90; Clinvar:1; Clinvar (benign):2 | ||||
chr19:11559189-11559336 | Common:1; Rare:53 | ||||
chr19:11597338-11597512 | Rare:55 | ||||
chr19:11738877-11739252 | Common:4; Rare:100 | ||||
chr19:12156673-12156879 | Common:1; Rare:46 | ||||
chr19:12365625-12365784 | Common:3; Rare:42 | ||||
chr19:12484776-12484923 | Rare:37 | ||||
chr19:12551400-12551690 | Common:2; Rare:77 | ||||
chr19:12610696-12610989 | Rare:95 | ||||
chr19:12666697-12666830 | Rare:53; Clinvar:4 | ||||
chr19:12681357-12681546 | Common:1; Rare:72 | ||||
chr19:12696582-12696705 | Rare:56 |