| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:41688947-41689070 | Common:1; Rare:9 | ||||
| chrX:41723879-41724181 | Rare:38 | ||||
| chrX:43656094-43656423 | Rare:60 | ||||
| chrX:44542796-44543034 | Common:1; Rare:48 | ||||
| chrX:44873468-44873795 | Rare:90; Clinvar (benign):2 | ||||
| chrX:44874104-44874187 | Rare:16 | ||||
| chrX:46545377-46545534 | Common:1; Rare:30; Clinvar (benign):1 | ||||
| chrX:47078380-47078495 | Common:1; Rare:12 | ||||
| chrX:47144474-47144858 | Common:2; Rare:84; Clinvar (benign):1 | ||||
| chrX:47145051-47145354 | Rare:44 | ||||
| chrX:47145462-47145573 | Rare:23 | ||||
| chrX:47218642-47218741 | Rare:54 | ||||
| chrX:47232920-47233052 | Rare:40 | ||||
| chrX:47233309-47233456 | Rare:24 | ||||
| chrX:47233640-47233830 | Common:1; Rare:24 |