Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:34999423-34999609 | Common:1; Rare:33 | ||||
chr19:34999840-34999953 | Common:1; Rare:17 | ||||
chr19:35000184-35000481 | Common:4; Rare:72 | ||||
chr19:35041579-35041765 | Rare:39 | ||||
chr19:35138643-35138883 | Rare:60 | ||||
chr19:35138994-35139176 | Common:2; Rare:37 | ||||
chr19:35139574-35139655 | Rare:18 | ||||
chr19:35155155-35155230 | Rare:15 | ||||
chr19:35248880-35249013 | Common:1; Rare:57 | ||||
chr19:35278573-35278790 | Common:2; Rare:51 | ||||
chr19:35545446-35545689 | Common:4; Rare:81 | ||||
chr19:35612676-35612824 | Common:1; Rare:50 | ||||
chr19:35628897-35629100 | Common:3; Rare:57 | ||||
chr19:35648093-35648401 | Common:1; Rare:70; Clinvar:1; Clinvar (benign):1 | ||||
chr19:35745397-35745697 | Rare:88 |