| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:120604623-120604686 | Rare:6 | ||||
| chrX:123733005-123733132 | Rare:21; Clinvar (benign):1 | ||||
| chrX:123960350-123960732 | Rare:28 | ||||
| chrX:123960760-123960903 | Rare:17 | ||||
| chrX:123961264-123961834 | Common:2; Rare:73 | ||||
| chrX:129540190-129540350 | Common:1; Rare:37 | ||||
| chrX:129738916-129739205 | Common:2; Rare:45 | ||||
| chrX:129779833-129779975 | Rare:22 | ||||
| chrX:129906069-129906201 | Rare:31 | ||||
| chrX:129982327-129982636 | Common:1; Rare:44 | ||||
| chrX:130110427-130110636 | Rare:49 | ||||
| chrX:130165689-130165908 | Rare:44; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chrX:132023168-132023385 | Rare:48 | ||||
| chrX:132217728-132218012 | Common:1; Rare:37 | ||||
| chrX:132219427-132219609 | Rare:22 |