Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:40605550-40605815 | Rare:94; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr19:40730975-40731300 | Common:6; Rare:68 | ||||
chr19:40737545-40737612 | Rare:8 | ||||
chr19:40812057-40812121 | Rare:9 | ||||
chr19:41500589-41500836 | Common:2; Rare:46 | ||||
chr19:42388590-42388691 | Rare:10 | ||||
chr19:42388835-42389015 | Common:1; Rare:44 | ||||
chr19:42389023-42389363 | Common:1; Rare:72 | ||||
chr19:42389403-42389704 | Common:2; Rare:63 | ||||
chr19:42396931-42397184 | Common:1; Rare:60 | ||||
chr19:42410755-42411017 | Rare:58 | ||||
chr19:44847594-44847747 | Common:1; Rare:32 | ||||
chr19:46860778-46861115 | Common:3; Rare:108 | ||||
chr19:46927210-46927477 | Rare:32 | ||||
chr19:47108048-47108156 | Rare:30 |