Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chrX:119852932-119853256 | Common:3; Rare:52; Clinvar (benign):3 | ||||
chrX:119871609-119871923 | Common:2; Rare:62; Clinvar (benign):3 | ||||
chrX:120560735-120560860 | Rare:18 | ||||
chrX:120561056-120561248 | Rare:39 | ||||
chrX:120561404-120561715 | Common:1; Rare:47 | ||||
chrX:120604037-120604152 | Rare:24 | ||||
chrX:120629934-120630344 | Common:4; Rare:83 | ||||
chrX:123733009-123733137 | Rare:21; Clinvar (benign):1 | ||||
chrX:123859610-123859905 | Common:2; Rare:45 | ||||
chrX:123960350-123960734 | Rare:28 | ||||
chrX:123961270-123961432 | Common:2; Rare:22 | ||||
chrX:123961566-123961843 | Rare:38 | ||||
chrX:129905977-129906201 | Rare:60 | ||||
chrX:130165735-130165908 | Rare:31; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chrX:132217726-132218012 | Common:1; Rare:37 |