Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:7533860-7534191 | Common:3; Rare:83; Clinvar (benign):1 | ||||
chr19:7535607-7535766 | Common:3; Rare:58 | ||||
chr19:7629535-7629848 | Common:5; Rare:111; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr19:7636953-7637152 | Common:2; Rare:59; Clinvar (benign):1 | ||||
chr19:8321294-8321653 | Common:2; Rare:156 | ||||
chr19:8390038-8390416 | Common:1; Rare:107 | ||||
chr19:8444805-8445109 | Common:2; Rare:138; Clinvar (benign):1 | ||||
chr19:8514098-8514226 | Common:2; Rare:39 | ||||
chr19:8832170-8832363 | Common:2; Rare:69 | ||||
chr19:9140296-9140432 | Common:1; Rare:36 | ||||
chr19:9435475-9435641 | Common:1; Rare:63 | ||||
chr19:9538578-9538756 | Common:1; Rare:53 | ||||
chr19:9584459-9584603 | Common:1; Rare:48 | ||||
chr19:9621178-9621570 | Common:3; Rare:113 | ||||
chr19:9675018-9675149 | Common:1; Rare:34 |