| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:23907873-23908169 | Rare:66 | ||||
| chrX:24149638-24149768 | Rare:25 | ||||
| chrX:30653115-30653437 | Common:2; Rare:83 | ||||
| chrX:37349173-37349396 | Common:2; Rare:33 | ||||
| chrX:38220789-38221023 | Rare:56 | ||||
| chrX:38327479-38327695 | Rare:57 | ||||
| chrX:43656117-43656356 | Rare:47 | ||||
| chrX:44542808-44543099 | Common:1; Rare:62 | ||||
| chrX:46545377-46545531 | Common:1; Rare:30; Clinvar (benign):1 | ||||
| chrX:46836696-46837069 | Rare:66; Clinvar:2; Clinvar (benign):1 | ||||
| chrX:47144507-47144813 | Common:1; Rare:65; Clinvar (benign):1 | ||||
| chrX:47145050-47145302 | Rare:37 | ||||
| chrX:47218090-47218247 | Common:1; Rare:18 | ||||
| chrX:47232920-47233040 | Rare:34 | ||||
| chrX:47233277-47233449 | Rare:28 |