| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:48696575-48696777 | Rare:44 | ||||
| chrX:48801359-48801424 | Common:1; Rare:7 | ||||
| chrX:48801547-48802216 | Common:2; Rare:116 | ||||
| chrX:48802503-48802545 | Rare:2 | ||||
| chrX:48911632-48911715 | Rare:21; Clinvar (benign):3 | ||||
| chrX:48919013-48919237 | Rare:38 | ||||
| chrX:48958271-48958414 | Rare:37 | ||||
| chrX:49002153-49002573 | Common:2; Rare:73 | ||||
| chrX:49073987-49074190 | Rare:49 | ||||
| chrX:49079831-49079972 | Rare:20 | ||||
| chrX:49171769-49171953 | Common:3; Rare:21 | ||||
| chrX:49269611-49269881 | Rare:67 | ||||
| chrX:49695957-49696030 | Rare:16 | ||||
| chrX:49922456-49922735 | Rare:63 | ||||
| chrX:50200330-50200482 | Rare:22 |