Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:42268247-42268602 | Rare:72 | ||||
chr19:42268704-42269035 | Rare:77 | ||||
chr19:42269636-42269816 | Common:1; Rare:39 | ||||
chr19:42283729-42284066 | Rare:111 | ||||
chr19:42294017-42294253 | Rare:68 | ||||
chr19:42301972-42302145 | Rare:47 | ||||
chr19:42302247-42302931 | Common:3; Rare:164 | ||||
chr19:42313259-42313493 | Common:2; Rare:60 | ||||
chr19:42325368-42325687 | Rare:90 | ||||
chr19:42352544-42352830 | Rare:57 | ||||
chr19:42423202-42423391 | Common:2; Rare:46 | ||||
chr19:42423514-42423753 | Common:4; Rare:89 | ||||
chr19:42423940-42424071 | Rare:25 | ||||
chr19:43527176-43527303 | Common:4; Rare:53; Clinvar:2; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
chr19:43533371-43533432 | Rare:18 |