Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:44663586-44663845 | Rare:123; Clinvar:8; Clinvar (benign):5 | ||||
chr15:44711367-44711611 | Rare:80; Clinvar:1; Clinvar (pathogenic):1 | ||||
chr15:45201091-45201133 | Common:1; Rare:19 | ||||
chr15:45587110-45587263 | Rare:26 | ||||
chr15:45587312-45587470 | Rare:47; Clinvar:4 | ||||
chr15:45587558-45587815 | Common:2; Rare:81 | ||||
chr15:48331170-48331453 | Common:4; Rare:90 | ||||
chr15:48645710-48645913 | Common:2; Rare:65; Clinvar (benign):1 | ||||
chr15:48878008-48878276 | Rare:102 | ||||
chr15:49046352-49046541 | Rare:80 | ||||
chr15:49155528-49155845 | Common:2; Rare:108 | ||||
chr15:49170088-49170286 | Rare:39 | ||||
chr15:49423111-49423404 | Common:1; Rare:49 | ||||
chr15:49620810-49621099 | Common:6; Rare:112 | ||||
chr15:50355074-50355509 | Common:3; Rare:173 |