Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:43754856-43755102 | Common:3; Rare:97 | ||||
chr19:44071991-44072181 | Common:1; Rare:43 | ||||
chr19:44094244-44094420 | Common:1; Rare:39 | ||||
chr19:44141410-44141717 | Common:3; Rare:43 | ||||
chr19:44304992-44305162 | Rare:46 | ||||
chr19:44356652-44356848 | Common:1; Rare:40 | ||||
chr19:44500477-44500649 | Common:3; Rare:52 | ||||
chr19:44643822-44643918 | Rare:27 | ||||
chr19:44748039-44748086 | Rare:7 | ||||
chr19:44757282-44757580 | Common:1; Rare:72; Clinvar:1 | ||||
chr19:44758014-44758272 | Common:1; Rare:48 | ||||
chr19:45406290-45406654 | Common:1; Rare:79 | ||||
chr19:45423454-45423790 | Common:2; Rare:70; Clinvar (benign):1 | ||||
chr19:45423832-45424012 | Common:2; Rare:38 | ||||
chr19:45506484-45506629 | Common:2; Rare:38 |