| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:48574250-48574558 | Common:2; Rare:92 | ||||
| chrX:48574865-48575007 | Rare:39 | ||||
| chrX:48696583-48696768 | Rare:41 | ||||
| chrX:48958320-48958682 | Rare:73 | ||||
| chrX:49002180-49002265 | Rare:26 | ||||
| chrX:49079822-49079946 | Rare:18 | ||||
| chrX:49186314-49186426 | Rare:18 | ||||
| chrX:49922350-49922665 | Common:1; Rare:74 | ||||
| chrX:51803019-51803112 | Rare:23 | ||||
| chrX:51893341-51893735 | Common:2; Rare:76 | ||||
| chrX:53422605-53422956 | Common:2; Rare:91; Clinvar (benign):1 | ||||
| chrX:53686299-53686466 | Rare:27 | ||||
| chrX:54530047-54530318 | Common:2; Rare:38 | ||||
| chrX:55000204-55000381 | Rare:32 | ||||
| chrX:55161097-55161262 | Rare:47 |