| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:37349173-37349398 | Common:2; Rare:33 | ||||
| chrX:37847503-37847688 | Common:1; Rare:47 | ||||
| chrX:38327450-38327598 | Rare:31 | ||||
| chrX:38801115-38801470 | Common:1; Rare:67 | ||||
| chrX:40580730-40581055 | Common:5; Rare:77; Clinvar (benign):3 | ||||
| chrX:40736154-40736245 | Common:2; Rare:14 | ||||
| chrX:41333810-41334203 | Common:4; Rare:101 | ||||
| chrX:43973387-43973583 | Common:1; Rare:30; Clinvar (benign):1 | ||||
| chrX:44542748-44543090 | Common:2; Rare:74 | ||||
| chrX:46545377-46545531 | Common:1; Rare:30; Clinvar (benign):1 | ||||
| chrX:46836686-46837027 | Rare:58; Clinvar:1 | ||||
| chrX:47078322-47078419 | Common:1; Rare:16 | ||||
| chrX:47144474-47144866 | Common:2; Rare:85; Clinvar (benign):1 | ||||
| chrX:47145068-47145301 | Rare:35 | ||||
| chrX:47232912-47233036 | Rare:36 |