| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:47078606-47078999 | Common:2; Rare:56 | ||||
| chrX:47144474-47144760 | Common:1; Rare:70; Clinvar (benign):1 | ||||
| chrX:47145005-47145325 | Rare:41 | ||||
| chrX:47218645-47218718 | Rare:38 | ||||
| chrX:47233320-47233456 | Rare:22 | ||||
| chrX:47233710-47233820 | Rare:18 | ||||
| chrX:47482556-47482670 | Common:5; Rare:25; Clinvar:2 | ||||
| chrX:47482928-47483032 | Rare:18 | ||||
| chrX:47483169-47483277 | Common:3; Rare:14 | ||||
| chrX:47560877-47561237 | Common:1; Rare:62 | ||||
| chrX:47659057-47659264 | Rare:59 | ||||
| chrX:47836632-47836953 | Common:1; Rare:69 | ||||
| chrX:48508821-48509032 | Common:1; Rare:44 | ||||
| chrX:48515730-48515953 | Rare:37; Clinvar:1 | ||||
| chrX:48574467-48574572 | Rare:43 |