Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:45587292-45587450 | Rare:48; Clinvar:6 | ||||
chr15:45587558-45587815 | Common:2; Rare:81 | ||||
chr15:45634916-45635084 | Rare:45 | ||||
chr15:48331368-48331476 | Rare:36 | ||||
chr15:48331890-48332272 | Common:6; Rare:121 | ||||
chr15:48645710-48645866 | Common:2; Rare:54; Clinvar (benign):1 | ||||
chr15:48878034-48878201 | Rare:66 | ||||
chr15:49046401-49046605 | Common:2; Rare:75 | ||||
chr15:49155528-49155838 | Common:2; Rare:105 | ||||
chr15:49170124-49170299 | Rare:38 | ||||
chr15:49620755-49621134 | Common:7; Rare:141 | ||||
chr15:50354712-50354998 | Rare:82 | ||||
chr15:50355063-50355513 | Common:3; Rare:179 | ||||
chr15:50424138-50424466 | Common:2; Rare:119 | ||||
chr15:50686744-50686914 | Common:3; Rare:74 |