| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:37847495-37847641 | Rare:37 | ||||
| chrX:38327440-38327620 | Rare:38 | ||||
| chrX:40580734-40581044 | Common:5; Rare:74; Clinvar (benign):3 | ||||
| chrX:40735274-40735663 | Rare:103 | ||||
| chrX:40735800-40736004 | Common:1; Rare:42 | ||||
| chrX:41334333-41334657 | Common:2; Rare:118 | ||||
| chrX:41346039-41346248 | Rare:41 | ||||
| chrX:46447159-46447344 | Rare:35 | ||||
| chrX:46545377-46545564 | Common:1; Rare:44; Clinvar (benign):1 | ||||
| chrX:47144668-47144813 | Rare:24 | ||||
| chrX:47145090-47145301 | Rare:31 | ||||
| chrX:47232903-47233036 | Rare:37 | ||||
| chrX:47233302-47233456 | Rare:26 | ||||
| chrX:47482548-47482669 | Common:5; Rare:26; Clinvar:2 | ||||
| chrX:47483151-47483237 | Common:1; Rare:12 |