| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:14873002-14873387 | Common:2; Rare:78; Clinvar:1; Clinvar (benign):2 | ||||
| chrX:16719857-16719896 | Rare:8 | ||||
| chrX:16870068-16870121 | Rare:8 | ||||
| chrX:18984351-18984465 | Rare:22 | ||||
| chrX:19670388-19670659 | Common:1; Rare:27 | ||||
| chrX:19887524-19887597 | Rare:2 | ||||
| chrX:20266592-20266804 | Common:2; Rare:54 | ||||
| chrX:21839465-21839772 | Common:2; Rare:75; Clinvar:1 | ||||
| chrX:23667646-23667807 | Rare:43 | ||||
| chrX:23782937-23783693 | Common:8; Rare:163 | ||||
| chrX:23785328-23785660 | Common:1; Rare:60 | ||||
| chrX:24054899-24055007 | Rare:42 | ||||
| chrX:24693806-24693957 | Common:1; Rare:27 | ||||
| chrX:38220805-38221044 | Rare:54 | ||||
| chrX:40735507-40735690 | Rare:52 |