Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:10333493-10333742 | Rare:85 | ||||
chr19:10339606-10339712 | Common:1; Rare:32 | ||||
chr19:10339760-10339944 | Rare:33 | ||||
chr19:10353256-10353407 | Common:1; Rare:25 | ||||
chr19:10353642-10353716 | Rare:21; Clinvar (pathogenic):1 | ||||
chr19:10354201-10354423 | Common:3; Rare:44; Clinvar (benign):1 | ||||
chr19:10380454-10380835 | Common:13; Rare:115; Clinvar:5 | ||||
chr19:10395037-10395441 | Common:1; Rare:125 | ||||
chr19:10420083-10420482 | Common:1; Rare:96 | ||||
chr19:10502672-10502927 | Rare:73 | ||||
chr19:10568772-10569233 | Common:3; Rare:120 | ||||
chr19:10587193-10587349 | Common:1; Rare:42 | ||||
chr19:10653780-10654486 | Common:5; Rare:297 | ||||
chr19:10654692-10655131 | Common:5; Rare:174 | ||||
chr19:10701270-10701602 | Rare:114 |