Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:45201094-45201153 | Common:1; Rare:29 | ||||
chr15:45378385-45378687 | Common:4; Rare:88; Clinvar:2; Clinvar (benign):11 | ||||
chr15:45430449-45430611 | Rare:37 | ||||
chr15:45522560-45522663 | Rare:24 | ||||
chr15:45587051-45587254 | Common:1; Rare:38 | ||||
chr15:45587300-45587487 | Rare:59; Clinvar:6; Clinvar (benign):1 | ||||
chr15:45587564-45587815 | Common:2; Rare:78 | ||||
chr15:45634929-45635086 | Rare:44 | ||||
chr15:48331383-48331453 | Rare:22 | ||||
chr15:48645710-48645880 | Common:2; Rare:56; Clinvar (benign):1 | ||||
chr15:48878004-48878374 | Rare:138 | ||||
chr15:49155525-49155877 | Common:2; Rare:115 | ||||
chr15:49423315-49423402 | Rare:10 | ||||
chr15:49620752-49621110 | Common:6; Rare:132 | ||||
chr15:50354920-50355009 | Rare:16 |