| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:38220696-38221044 | Common:3; Rare:96 | ||||
| chrX:40580754-40581078 | Common:5; Rare:76; Clinvar (benign):3 | ||||
| chrX:40735294-40735704 | Rare:101 | ||||
| chrX:40735791-40735924 | Common:1; Rare:30 | ||||
| chrX:41333816-41334175 | Common:2; Rare:90 | ||||
| chrX:41334505-41334657 | Rare:64 | ||||
| chrX:44542768-44543090 | Common:1; Rare:70 | ||||
| chrX:46447181-46447338 | Rare:27 | ||||
| chrX:46545380-46545556 | Rare:38 | ||||
| chrX:46836717-46837090 | Rare:69; Clinvar:3; Clinvar (benign):1 | ||||
| chrX:46912247-46912328 | Rare:15 | ||||
| chrX:47144474-47144812 | Common:1; Rare:76; Clinvar (benign):1 | ||||
| chrX:47145077-47145349 | Rare:41 | ||||
| chrX:47190624-47190906 | Rare:41 | ||||
| chrX:47232914-47233046 | Rare:40 |