Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chrX:119468216-119468596 | Common:3; Rare:112 | ||||
chrX:119469083-119469138 | Rare:13 | ||||
chrX:119574374-119574581 | Rare:47 | ||||
chrX:119791588-119791979 | Common:2; Rare:105 | ||||
chrX:119852932-119853306 | Common:4; Rare:61; Clinvar (benign):3 | ||||
chrX:119871523-119871904 | Common:2; Rare:69; Clinvar (benign):2 | ||||
chrX:123733025-123733146 | Rare:19 | ||||
chrX:123961264-123961435 | Common:2; Rare:22 | ||||
chrX:123961565-123961834 | Rare:37 | ||||
chrX:129540081-129540314 | Common:3; Rare:37 | ||||
chrX:129906073-129906201 | Rare:31 | ||||
chrX:132023145-132023306 | Rare:41 | ||||
chrX:132217719-132218012 | Common:1; Rare:39 | ||||
chrX:132218044-132218297 | Rare:29 | ||||
chrX:135022468-135022577 | Rare:34 |