| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:23782961-23783269 | Common:5; Rare:68 | ||||
| chrX:24054901-24054999 | Rare:37 | ||||
| chrX:24465066-24465337 | Common:4; Rare:79 | ||||
| chrX:30653134-30653428 | Common:2; Rare:78 | ||||
| chrX:37847506-37847657 | Rare:40 | ||||
| chrX:38327450-38327682 | Rare:55 | ||||
| chrX:41333617-41333934 | Common:4; Rare:75 | ||||
| chrX:41689003-41689070 | Common:1; Rare:6 | ||||
| chrX:43656066-43656414 | Rare:62 | ||||
| chrX:46545377-46545544 | Common:1; Rare:34; Clinvar (benign):1 | ||||
| chrX:47144599-47144794 | Rare:40 | ||||
| chrX:47145043-47145392 | Rare:56 | ||||
| chrX:47233320-47233449 | Rare:22 | ||||
| chrX:47659103-47659246 | Rare:42 | ||||
| chrX:47836791-47836924 | Common:1; Rare:35 |