Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:19192128-19192245 | Common:1; Rare:36 | ||||
chr19:19320480-19320844 | Common:4; Rare:130 | ||||
chr19:19516163-19516287 | Rare:77; Clinvar:1; Clinvar (pathogenic):1 | ||||
chr19:19900795-19900953 | Rare:37 | ||||
chr19:20923116-20923248 | Rare:29 | ||||
chr19:32971922-32972250 | Common:4; Rare:93 | ||||
chr19:34172342-34172551 | Rare:91 | ||||
chr19:34428319-34428435 | Rare:50 | ||||
chr19:34677585-34677719 | Common:2; Rare:36 | ||||
chr19:35155141-35155251 | Rare:24 | ||||
chr19:35545483-35545689 | Common:4; Rare:69 | ||||
chr19:35628931-35629078 | Common:1; Rare:42 | ||||
chr19:35745397-35745695 | Rare:88 | ||||
chr19:36014214-36014542 | Common:2; Rare:87 | ||||
chr19:36114852-36114973 | Common:1; Rare:53 |