Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:39391125-39391418 | Common:1; Rare:122 | ||||
chr19:40348510-40348740 | Common:3; Rare:76 | ||||
chr19:40716883-40717152 | Common:1; Rare:83 | ||||
chr19:41262326-41262566 | Rare:45 | ||||
chr19:41264793-41265104 | Common:2; Rare:62 | ||||
chr19:41353611-41353633 | Rare:3 | ||||
chr19:41397306-41397841 | Common:12; Rare:167; Clinvar (benign):4 | ||||
chr19:41860113-41860525 | Common:5; Rare:155; Clinvar:4; Clinvar (benign):2 | ||||
chr19:42075833-42076194 | Rare:98 | ||||
chr19:42132393-42132618 | Rare:51 | ||||
chr19:42302411-42302437 | Rare:7 | ||||
chr19:43575462-43575807 | Common:2; Rare:93 | ||||
chr19:43596117-43596423 | Common:2; Rare:92 | ||||
chr19:43619577-43619783 | Common:3; Rare:69 | ||||
chr19:43670152-43670344 | Common:2; Rare:45 |