| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:37847517-37847647 | Rare:34 | ||||
| chrX:38561339-38561557 | Common:3; Rare:54; Clinvar (benign):1 | ||||
| chrX:38801254-38801470 | Common:1; Rare:36 | ||||
| chrX:40580734-40581021 | Common:4; Rare:69; Clinvar (benign):1 | ||||
| chrX:40735791-40736023 | Common:1; Rare:46 | ||||
| chrX:46545362-46545574 | Common:1; Rare:51; Clinvar (benign):1 | ||||
| chrX:47144474-47144502 | Rare:10 | ||||
| chrX:47144617-47144812 | Rare:34 | ||||
| chrX:47145097-47145311 | Rare:32 | ||||
| chrX:47232931-47233056 | Rare:36 | ||||
| chrX:47233320-47233456 | Rare:22 | ||||
| chrX:47482548-47482657 | Common:5; Rare:24; Clinvar:2 | ||||
| chrX:47560916-47561215 | Common:1; Rare:55 | ||||
| chrX:48003979-48004137 | Rare:41 | ||||
| chrX:48071097-48071233 | Rare:8 |