| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:123961264-123961432 | Common:2; Rare:22 | ||||
| chrX:123961553-123961850 | Rare:43 | ||||
| chrX:129523198-129523288 | Rare:30 | ||||
| chrX:129523290-129523641 | Common:4; Rare:78 | ||||
| chrX:129540182-129540427 | Common:1; Rare:49 | ||||
| chrX:129906002-129906212 | Rare:57 | ||||
| chrX:129982307-129982643 | Common:1; Rare:49 | ||||
| chrX:130165660-130165922 | Rare:51; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chrX:132023104-132023380 | Rare:59 | ||||
| chrX:132217734-132218297 | Common:1; Rare:71 | ||||
| chrX:133415144-133415251 | Rare:17 | ||||
| chrX:135022434-135022696 | Rare:63 | ||||
| chrX:135032503-135032805 | Rare:51 | ||||
| chrX:135032817-135033066 | Rare:38 | ||||
| chrX:135052100-135052361 | Common:2; Rare:72 |