| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:23783589-23783731 | Common:1; Rare:31 | ||||
| chrX:23907703-23907792 | Common:1; Rare:20 | ||||
| chrX:23907842-23908068 | Rare:43 | ||||
| chrX:24054888-24055015 | Rare:46 | ||||
| chrX:24149570-24149774 | Rare:33 | ||||
| chrX:24465034-24465369 | Common:4; Rare:95 | ||||
| chrX:24693762-24693977 | Common:1; Rare:38 | ||||
| chrX:30653162-30653504 | Common:2; Rare:87 | ||||
| chrX:37847506-37847699 | Common:1; Rare:48 | ||||
| chrX:38327471-38327682 | Rare:53 | ||||
| chrX:38801237-38801516 | Common:2; Rare:55 | ||||
| chrX:41085711-41086025 | Common:1; Rare:76 | ||||
| chrX:43656086-43656402 | Rare:60 | ||||
| chrX:43743493-43743864 | Common:2; Rare:41 | ||||
| chrX:46545377-46545549 | Common:1; Rare:35; Clinvar (benign):1 |