Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:21500218-21500515 | Common:5; Rare:55 | ||||
chr14:22769519-22769931 | Common:1; Rare:86; Clinvar (pathogenic):1 | ||||
chr14:22771057-22771347 | Common:2; Rare:102 | ||||
chr14:23022857-23023059 | Rare:35 | ||||
chr14:23058383-23058650 | Common:1; Rare:73 | ||||
chr14:27377760-27377997 | Common:1; Rare:49 | ||||
chr14:27673230-27673335 | Common:1; Rare:37 | ||||
chr14:27845275-27845481 | Common:3; Rare:62 | ||||
chr14:27845629-27845744 | Common:2; Rare:39 | ||||
chr14:30929419-30929774 | Common:1; Rare:63 | ||||
chr14:31107231-31107365 | Rare:19 | ||||
chr14:32417951-32418356 | Rare:63 | ||||
chr14:33520212-33520405 | Common:1; Rare:34 | ||||
chr14:33556984-33557225 | Common:5; Rare:51 | ||||
chr14:34969176-34969283 | Common:1; Rare:13 |