| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:48356650-48357019 | Common:5; Rare:93 | ||||
| chrX:48475874-48476273 | Rare:68 | ||||
| chrX:48508814-48509036 | Common:1; Rare:46 | ||||
| chrX:48574429-48574581 | Rare:58 | ||||
| chrX:48574869-48574956 | Rare:26 | ||||
| chrX:48801877-48802238 | Common:1; Rare:54 | ||||
| chrX:48898036-48898265 | Common:2; Rare:33 | ||||
| chrX:48911637-48911715 | Rare:19; Clinvar (benign):3 | ||||
| chrX:49002200-49002265 | Rare:23 | ||||
| chrX:49079854-49079953 | Rare:15 | ||||
| chrX:49186314-49186457 | Common:1; Rare:23 | ||||
| chrX:53422202-53422329 | Rare:31 | ||||
| chrX:53422616-53422925 | Common:2; Rare:82; Clinvar (benign):1 | ||||
| chrX:53684253-53684472 | Rare:46 | ||||
| chrX:54440249-54440465 | Rare:42 |