| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:23743175-23743612 | Common:8; Rare:78 | ||||
| chrX:23907712-23907823 | Common:1; Rare:29 | ||||
| chrX:23907824-23908068 | Rare:45 | ||||
| chrX:24054625-24054987 | Common:1; Rare:80 | ||||
| chrX:30653154-30653425 | Common:2; Rare:72 | ||||
| chrX:38327479-38327699 | Rare:58 | ||||
| chrX:46545377-46545525 | Common:1; Rare:27; Clinvar (benign):1 | ||||
| chrX:47144668-47144813 | Rare:24 | ||||
| chrX:47145097-47145301 | Rare:31 | ||||
| chrX:47483169-47483277 | Common:3; Rare:14 | ||||
| chrX:47560986-47561216 | Common:1; Rare:39 | ||||
| chrX:48476089-48476252 | Rare:33 | ||||
| chrX:48508902-48509027 | Rare:20 | ||||
| chrX:48958363-48958694 | Rare:55 | ||||
| chrX:49002207-49002360 | Rare:41 |