| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:24054882-24055005 | Rare:46 | ||||
| chrX:38220810-38221028 | Rare:51 | ||||
| chrX:38327504-38327653 | Rare:38 | ||||
| chrX:40735538-40735682 | Rare:40 | ||||
| chrX:46545403-46545564 | Rare:38 | ||||
| chrX:47144681-47144738 | Rare:12 | ||||
| chrX:47145100-47145308 | Rare:32 | ||||
| chrX:47483169-47483342 | Common:3; Rare:17 | ||||
| chrX:48508861-48509038 | Rare:34 | ||||
| chrX:48574880-48575007 | Rare:35 | ||||
| chrX:48911613-48911691 | Rare:20; Clinvar (benign):4 | ||||
| chrX:55000207-55000425 | Common:1; Rare:52 | ||||
| chrX:57121472-57121855 | Common:2; Rare:87 | ||||
| chrX:65034717-65034826 | Common:1; Rare:23 | ||||
| chrX:68498961-68499064 | Rare:26 |