| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:54440271-54440466 | Rare:42 | ||||
| chrX:54530064-54530303 | Common:2; Rare:35 | ||||
| chrX:55000194-55000390 | Rare:38 | ||||
| chrX:55161152-55161249 | Rare:28 | ||||
| chrX:56729458-56729530 | Common:1; Rare:9 | ||||
| chrX:57121428-57121599 | Common:1; Rare:41 | ||||
| chrX:63785130-63785227 | Rare:24; Clinvar (pathogenic):1 | ||||
| chrX:64205697-64205966 | Common:1; Rare:50 | ||||
| chrX:65034708-65034859 | Common:1; Rare:32 | ||||
| chrX:66162372-66162700 | Common:2; Rare:45 | ||||
| chrX:68498961-68499059 | Rare:22 | ||||
| chrX:68828837-68829034 | Rare:40 | ||||
| chrX:68829309-68829573 | Common:2; Rare:42 | ||||
| chrX:70289865-70290112 | Rare:44 | ||||
| chrX:70423200-70423351 | Common:1; Rare:17 |