| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:135973695-135973850 | Rare:55 | ||||
| chrX:135985344-135985503 | Rare:46; Clinvar (benign):4 | ||||
| chrX:139204997-139205195 | Rare:36 | ||||
| chrX:141177076-141177320 | Common:1; Rare:33 | ||||
| chrX:149540817-149541048 | Common:4; Rare:44 | ||||
| chrX:150983064-150983373 | Common:3; Rare:64 | ||||
| chrX:151397057-151397273 | Common:4; Rare:109 | ||||
| chrX:152830712-152831072 | Common:2; Rare:66 | ||||
| chrX:152941509-152941681 | Common:1; Rare:43 | ||||
| chrX:153599081-153599350 | Common:13; Rare:55 | ||||
| chrX:153794316-153794693 | Common:1; Rare:117; Clinvar (benign):2 | ||||
| chrX:153972429-153972782 | Common:2; Rare:109 | ||||
| chrX:154409148-154409427 | Rare:46 | ||||
| chrX:154428457-154428698 | Common:2; Rare:41 | ||||
| chrX:154516175-154516537 | Common:4; Rare:76 |