Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:7535543-7535747 | Common:3; Rare:69; Clinvar:2 | ||||
chr19:7629520-7629836 | Common:5; Rare:113; Clinvar (benign):2 | ||||
chr19:7637007-7637158 | Common:2; Rare:48; Clinvar (benign):1 | ||||
chr19:7943625-7943988 | Rare:102 | ||||
chr19:8308275-8308661 | Common:4; Rare:126; Clinvar:1; Clinvar (benign):1 | ||||
chr19:8321324-8321675 | Common:2; Rare:148 | ||||
chr19:8364022-8364162 | Common:1; Rare:36 | ||||
chr19:8390068-8390419 | Common:1; Rare:99 | ||||
chr19:8444818-8445109 | Common:2; Rare:131; Clinvar (benign):1 | ||||
chr19:8514138-8514256 | Common:1; Rare:34 | ||||
chr19:9435512-9435614 | Rare:41 | ||||
chr19:9538574-9538707 | Common:1; Rare:37 | ||||
chr19:9621168-9621548 | Common:4; Rare:109 | ||||
chr19:9621783-9621948 | Common:1; Rare:32 | ||||
chr19:9675022-9675149 | Rare:33 |