Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:48966317-48966727 | Rare:131; Clinvar:2; Clinvar (pathogenic):1 | ||||
chr19:49090291-49090519 | Rare:51 | ||||
chr19:49098422-49098707 | Rare:69 | ||||
chr19:49107340-49107663 | Rare:78 | ||||
chr19:49108589-49108890 | Common:3; Rare:77 | ||||
chr19:49491403-49491726 | Common:8; Rare:114 | ||||
chr19:49492296-49492410 | Rare:35 | ||||
chr19:49592233-49592379 | Common:1; Rare:47 | ||||
chr19:49806446-49806881 | Common:3; Rare:114 | ||||
chr19:49818962-49819209 | Common:2; Rare:57 | ||||
chr19:49933928-49934125 | Common:2; Rare:40 | ||||
chr19:50381897-50382024 | Common:2; Rare:50 | ||||
chr19:51691633-51691820 | Common:3; Rare:27 | ||||
chr19:53102361-53102509 | Rare:36 | ||||
chr19:53865278-53865382 | Rare:22 |