| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:47629884-47630131 | Common:2; Rare:30 | ||||
| chrX:47659107-47659264 | Rare:45 | ||||
| chrX:47836791-47836953 | Common:1; Rare:38 | ||||
| chrX:48003960-48004134 | Rare:46 | ||||
| chrX:48475900-48476256 | Rare:62 | ||||
| chrX:48508848-48509027 | Common:1; Rare:37 | ||||
| chrX:48574875-48575250 | Common:3; Rare:90 | ||||
| chrX:48696584-48696777 | Rare:43 | ||||
| chrX:48911632-48911711 | Rare:19; Clinvar (benign):3 | ||||
| chrX:48919013-48919265 | Rare:40 | ||||
| chrX:48958320-48958406 | Rare:25 | ||||
| chrX:49073977-49074165 | Rare:49 | ||||
| chrX:49079800-49079922 | Rare:15 | ||||
| chrX:49171769-49172084 | Common:4; Rare:50 | ||||
| chrX:49186293-49186482 | Common:1; Rare:33 |