| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:119468209-119468607 | Common:3; Rare:113 | ||||
| chrX:119469043-119469337 | Rare:75 | ||||
| chrX:119574428-119574594 | Rare:39 | ||||
| chrX:119791572-119791978 | Common:2; Rare:108 | ||||
| chrX:119871555-119871983 | Common:2; Rare:77; Clinvar (benign):3 | ||||
| chrX:119943263-119943321 | Common:1; Rare:13 | ||||
| chrX:120468934-120469070 | Common:1; Rare:17 | ||||
| chrX:120560777-120560859 | Rare:12 | ||||
| chrX:120560943-120561138 | Rare:34 | ||||
| chrX:120604061-120604164 | Rare:25 | ||||
| chrX:120629930-120630267 | Common:4; Rare:65 | ||||
| chrX:123733018-123733146 | Rare:20 | ||||
| chrX:123960350-123960748 | Rare:28 | ||||
| chrX:123961264-123961432 | Common:2; Rare:22 | ||||
| chrX:123961492-123961812 | Rare:45 |