Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:27793370-27793498 | Common:1; Rare:32 | ||||
chr19:27793681-27794027 | Rare:89 | ||||
chr19:36797323-36797534 | Rare:40 | ||||
chr19:41500618-41500790 | Common:1; Rare:32 | ||||
chr19:41531561-41531708 | Common:1; Rare:35 | ||||
chr19:42396907-42397184 | Common:1; Rare:66 | ||||
chr19:46860839-46861114 | Common:3; Rare:88 | ||||
chr19:48873016-48873259 | Common:2; Rare:43 | ||||
chr19:48966390-48966673 | Rare:91; Clinvar:1 | ||||
chr19:49009806-49010064 | Common:1; Rare:99 | ||||
chr19:49090328-49090508 | Rare:44 | ||||
chr19:52923411-52923549 | Common:3; Rare:54 | ||||
chr2:19933425-19933721 | Common:4; Rare:59; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr2:55282204-55282368 | Common:5; Rare:57 | ||||
chr2:55989489-55989666 | Common:3; Rare:31 |