| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:103688006-103688276 | Common:1; Rare:32 | ||||
| chrX:104156896-104157047 | Common:1; Rare:25 | ||||
| chrX:107716432-107716616 | Common:1; Rare:25 | ||||
| chrX:108091513-108091818 | Rare:80 | ||||
| chrX:108439457-108439898 | Common:3; Rare:98 | ||||
| chrX:110317931-110318248 | Rare:82 | ||||
| chrX:118345861-118346137 | Common:2; Rare:47 | ||||
| chrX:119468222-119468456 | Common:3; Rare:68 | ||||
| chrX:119574382-119574594 | Rare:47 | ||||
| chrX:119791594-119791721 | Rare:52 | ||||
| chrX:119871673-119871911 | Common:1; Rare:56; Clinvar (benign):3 | ||||
| chrX:123961238-123961432 | Common:2; Rare:28 | ||||
| chrX:123961543-123961834 | Rare:42 | ||||
| chrX:130165689-130165972 | Rare:62; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chrX:131579076-131579330 | Common:1; Rare:58 |