| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:41333108-41333538 | Rare:104 | ||||
| chrX:41333810-41333974 | Common:2; Rare:42 | ||||
| chrX:41334505-41334657 | Rare:64 | ||||
| chrX:43656152-43656328 | Rare:41 | ||||
| chrX:43973384-43973604 | Common:1; Rare:33; Clinvar (benign):1 | ||||
| chrX:44542740-44543061 | Common:2; Rare:72 | ||||
| chrX:44873028-44873199 | Rare:29 | ||||
| chrX:46447139-46447338 | Rare:38 | ||||
| chrX:46545371-46545547 | Common:1; Rare:36; Clinvar (benign):1 | ||||
| chrX:46836696-46837031 | Rare:57; Clinvar:1 | ||||
| chrX:47144449-47144843 | Common:7; Rare:96; Clinvar (benign):1 | ||||
| chrX:47145089-47145325 | Rare:34 | ||||
| chrX:47145419-47145570 | Common:2; Rare:27 | ||||
| chrX:47193707-47193967 | Common:1; Rare:47; Clinvar:1 | ||||
| chrX:47194244-47194303 | Common:1; Rare:5 |