Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:44812223-44812545 | Common:3; Rare:117; Clinvar (pathogenic):1 | ||||
chr19:44847612-44847657 | Rare:10 | ||||
chr19:46860833-46861133 | Common:3; Rare:96 | ||||
chr19:48966310-48966642 | Rare:101; Clinvar (pathogenic):2 | ||||
chr19:49090311-49090519 | Rare:48 | ||||
chr19:49200429-49200781 | Common:4; Rare:148; Clinvar:8; Clinvar (benign):2 | ||||
chr19:49491525-49491783 | Common:1; Rare:86 | ||||
chr19:50050982-50051007 | Rare:6 | ||||
chr19:50051009-50051086 | Rare:18 | ||||
chr19:50856098-50856219 | Common:1; Rare:27 | ||||
chr19:50858973-50859318 | Common:8; Rare:65 | ||||
chr19:50859322-50859779 | Common:12; Rare:117 | ||||
chr19:51976024-51976293 | Rare:46 | ||||
chr19:52923398-52923484 | Common:2; Rare:38 | ||||
chr19:52942549-52942789 | Common:8; Rare:86 |