| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:48574235-48574558 | Common:3; Rare:169 | ||||
| chrX:48574860-48574963 | Rare:29 | ||||
| chrX:48574866-48574999 | Rare:38 | ||||
| chrX:48589840-48590110 | Common:6; Rare:90 | ||||
| chrX:48676320-48676648 | Common:2; Rare:140 | ||||
| chrX:48696584-48696791 | Rare:95 | ||||
| chrX:48801500-48802220 | Common:4; Rare:183 | ||||
| chrX:48835543-48835689 | Rare:19 | ||||
| chrX:48835820-48836070 | Common:1; Rare:70 | ||||
| chrX:48911609-48911725 | Rare:54; Clinvar (benign):8 | ||||
| chrX:48911920-48912094 | Rare:32 | ||||
| chrX:48957553-48957714 | Rare:55 | ||||
| chrX:48957825-48958154 | Common:1; Rare:97 | ||||
| chrX:49002171-49002291 | Rare:61 | ||||
| chrX:49043102-49044074 | Common:4; Rare:318 |