| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:40097457-40097579 | Rare:12 | ||||
| chrX:40735910-40735925 | Rare:1 | ||||
| chrX:41334009-41334183 | Common:1; Rare:38 | ||||
| chrX:44542814-44543087 | Common:1; Rare:55 | ||||
| chrX:46447165-46447338 | Rare:32 | ||||
| chrX:46545387-46545564 | Rare:42 | ||||
| chrX:47144474-47144788 | Common:1; Rare:74; Clinvar (benign):1 | ||||
| chrX:47145089-47145301 | Rare:31 | ||||
| chrX:47232903-47233036 | Rare:37 | ||||
| chrX:47482579-47482665 | Common:5; Rare:19; Clinvar:2 | ||||
| chrX:47483169-47483310 | Common:3; Rare:16 | ||||
| chrX:48003964-48004137 | Rare:46 | ||||
| chrX:48476125-48476216 | Rare:18 | ||||
| chrX:48521573-48521868 | Common:1; Rare:48 | ||||
| chrX:48574869-48574907 | Rare:12 |