Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:49527861-49528031 | Common:3; Rare:53 | ||||
chr19:49580528-49580620 | Rare:32 | ||||
chr19:49665765-49666034 | Common:2; Rare:133; Clinvar (pathogenic):1 | ||||
chr19:49877341-49877717 | Common:1; Rare:93 | ||||
chr19:49878031-49878136 | Common:1; Rare:32 | ||||
chr19:49929458-49929832 | Common:7; Rare:131 | ||||
chr19:50384149-50384380 | Common:2; Rare:91; Clinvar:1; Clinvar (benign):2 | ||||
chr19:50476242-50476547 | Rare:144 | ||||
chr19:50983883-50984197 | Common:1; Rare:89 | ||||
chr19:51019696-51019965 | Common:5; Rare:49 | ||||
chr19:51026564-51026756 | Common:2; Rare:53 | ||||
chr19:51751858-51751987 | Common:2; Rare:28 | ||||
chr19:51887874-51888121 | Rare:85 | ||||
chr19:52008153-52008290 | Rare:43 | ||||
chr19:52028345-52028451 | Common:3; Rare:21 |