Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chrX:40580700-40581021 | Common:4; Rare:73; Clinvar (benign):1 | ||||
chrX:41085219-41085469 | Common:3; Rare:72 | ||||
chrX:43656060-43656399 | Rare:62 | ||||
chrX:46545385-46545556 | Rare:37 | ||||
chrX:47144650-47145232 | Common:1; Rare:80 | ||||
chrX:47233310-47233459 | Rare:24 | ||||
chrX:47483169-47483252 | Common:2; Rare:12 | ||||
chrX:47582255-47582471 | Rare:33 | ||||
chrX:47650529-47650762 | Common:3; Rare:75 | ||||
chrX:47659115-47659270 | Rare:45 | ||||
chrX:47836791-47836953 | Common:1; Rare:38 | ||||
chrX:48003979-48004137 | Rare:41 | ||||
chrX:48468294-48468487 | Common:1; Rare:25 | ||||
chrX:48476089-48476332 | Rare:45 | ||||
chrX:48508870-48508999 | Rare:20 |