| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:24149638-24149794 | Rare:32 | ||||
| chrX:30653176-30653425 | Common:2; Rare:66 | ||||
| chrX:37349030-37349404 | Common:2; Rare:55 | ||||
| chrX:37847486-37847657 | Rare:42 | ||||
| chrX:38327472-38327575 | Rare:21 | ||||
| chrX:40580700-40581041 | Common:5; Rare:78; Clinvar (benign):3 | ||||
| chrX:40735814-40736022 | Common:1; Rare:38 | ||||
| chrX:41085747-41085854 | Rare:28 | ||||
| chrX:44542766-44543090 | Common:1; Rare:71 | ||||
| chrX:46447183-46447341 | Rare:28 | ||||
| chrX:46545380-46545574 | Rare:46 | ||||
| chrX:47144520-47144816 | Common:2; Rare:61; Clinvar (benign):1 | ||||
| chrX:47145092-47145311 | Rare:32 | ||||
| chrX:47232920-47233036 | Rare:32 | ||||
| chrX:47233250-47233449 | Rare:35 |