| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:46545377-46545533 | Common:1; Rare:30; Clinvar (benign):1 | ||||
| chrX:47144474-47144736 | Common:1; Rare:67; Clinvar (benign):1 | ||||
| chrX:47145074-47145338 | Rare:40 | ||||
| chrX:47232912-47233116 | Rare:70 | ||||
| chrX:47233292-47233440 | Rare:26 | ||||
| chrX:47240603-47240876 | Rare:54 | ||||
| chrX:47482548-47482665 | Common:5; Rare:26; Clinvar:2 | ||||
| chrX:47483169-47483243 | Common:1; Rare:11 | ||||
| chrX:47582265-47582471 | Rare:33 | ||||
| chrX:47619470-47619624 | Common:2; Rare:29; Clinvar:2; Clinvar (benign):2 | ||||
| chrX:47619829-47620130 | Common:1; Rare:55 | ||||
| chrX:47659000-47659235 | Rare:66 | ||||
| chrX:47836791-47836953 | Common:1; Rare:38 | ||||
| chrX:48003953-48004214 | Common:2; Rare:72 | ||||
| chrX:48476080-48476263 | Rare:36 |