| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:118346375-118346527 | Rare:30 | ||||
| chrX:119468260-119468554 | Common:2; Rare:96 | ||||
| chrX:119574373-119574610 | Rare:52 | ||||
| chrX:119791560-119791971 | Common:2; Rare:106 | ||||
| chrX:119852924-119853221 | Common:3; Rare:49; Clinvar (benign):3 | ||||
| chrX:119871621-119871914 | Common:2; Rare:61; Clinvar (benign):3 | ||||
| chrX:120561395-120561715 | Common:1; Rare:51 | ||||
| chrX:120603796-120604152 | Rare:67 | ||||
| chrX:120629938-120630337 | Common:4; Rare:79 | ||||
| chrX:123859638-123859854 | Common:1; Rare:28 | ||||
| chrX:123961292-123961432 | Common:2; Rare:21 | ||||
| chrX:123961480-123961812 | Rare:46 | ||||
| chrX:129905941-129906208 | Rare:70 | ||||
| chrX:130165703-130165927 | Rare:42; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chrX:130268781-130269012 | Common:1; Rare:69 |