Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:40775410-40775562 | Common:2; Rare:44 | ||||
chr19:40798941-40799198 | Common:5; Rare:98 | ||||
chr19:41397332-41397477 | Common:3; Rare:42 | ||||
chr19:41860121-41860278 | Common:1; Rare:62; Clinvar:2; Clinvar (benign):1 | ||||
chr19:43670140-43670309 | Common:2; Rare:39 | ||||
chr19:44356685-44356829 | Common:1; Rare:23 | ||||
chr19:45406390-45406682 | Common:1; Rare:77 | ||||
chr19:46346951-46347099 | Common:3; Rare:45 | ||||
chr19:47256460-47256568 | Rare:39 | ||||
chr19:47349086-47349361 | Rare:76 | ||||
chr19:47484147-47484300 | Common:2; Rare:53; Clinvar:1 | ||||
chr19:48170270-48170669 | Common:2; Rare:111 | ||||
chr19:48619139-48619428 | Rare:92 | ||||
chr19:48993292-48993561 | Common:3; Rare:111; Clinvar:1; Clinvar (benign):2 | ||||
chr19:49085130-49085515 | Common:3; Rare:159 |