Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:43619582-43619639 | Rare:24 | ||||
chr19:43754901-43755102 | Common:3; Rare:69 | ||||
chr19:43935238-43935397 | Common:3; Rare:45 | ||||
chr19:44094148-44094420 | Common:1; Rare:67 | ||||
chr19:44141410-44141588 | Common:2; Rare:24 | ||||
chr19:44164925-44165141 | Common:1; Rare:53 | ||||
chr19:44955237-44955398 | Common:2; Rare:46 | ||||
chr19:45038943-45039097 | Rare:53 | ||||
chr19:45079161-45079322 | Rare:42 | ||||
chr19:45370544-45370731 | Common:2; Rare:57 | ||||
chr19:45406341-45406687 | Common:2; Rare:86 | ||||
chr19:45423502-45423712 | Common:2; Rare:46; Clinvar (benign):1 | ||||
chr19:45423848-45423992 | Common:2; Rare:32 | ||||
chr19:45469191-45469479 | Common:1; Rare:91 | ||||
chr19:47112166-47112505 | Rare:115 |