| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:118974916-118974960 | Rare:10 | ||||
| chrX:119468216-119468558 | Common:3; Rare:108 | ||||
| chrX:119469090-119469284 | Rare:56 | ||||
| chrX:119574364-119574612 | Rare:55 | ||||
| chrX:119605843-119606119 | Rare:39 | ||||
| chrX:119791585-119791985 | Common:2; Rare:108 | ||||
| chrX:119871617-119871994 | Common:2; Rare:75; Clinvar (benign):3 | ||||
| chrX:119943565-119943852 | Rare:56 | ||||
| chrX:120560473-120560860 | Rare:61; Clinvar:2 | ||||
| chrX:120604047-120604152 | Rare:22 | ||||
| chrX:120629938-120630356 | Common:5; Rare:85 | ||||
| chrX:123733021-123733105 | Rare:15 | ||||
| chrX:123960350-123960726 | Rare:28 | ||||
| chrX:123961281-123961435 | Common:2; Rare:21 | ||||
| chrX:123961565-123961845 | Rare:38 |