Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:41331848-41332219 | Rare:81; Clinvar (benign):1 | ||||
chr19:41353042-41353204 | Common:2; Rare:35 | ||||
chr19:41869745-41870013 | Common:2; Rare:65; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr19:45767459-45767615 | Rare:47 | ||||
chr19:45859262-45859314 | Rare:15 | ||||
chr19:46776970-46777216 | Common:1; Rare:61 | ||||
chr19:46860804-46861126 | Common:3; Rare:105 | ||||
chr19:47243079-47243402 | Common:4; Rare:79 | ||||
chr19:48966395-48966624 | Rare:69 | ||||
chr19:53876397-53876589 | Common:1; Rare:40 | ||||
chr19:53961029-53961122 | Common:1; Rare:19 | ||||
chr19:55230358-55230682 | Common:3; Rare:128 | ||||
chr19:55607262-55607436 | Common:1; Rare:36 | ||||
chr19:57296494-57296766 | Common:1; Rare:49 | ||||
chr19:58346904-58347124 | Common:1; Rare:66 |