| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:134797056-134797422 | Rare:111 | ||||
| chrX:134807057-134807338 | Common:2; Rare:82 | ||||
| chrX:134915177-134915422 | Common:2; Rare:65 | ||||
| chrX:134990834-134991103 | Common:1; Rare:72 | ||||
| chrX:135032195-135032383 | Rare:80 | ||||
| chrX:135052086-135052347 | Common:3; Rare:129 | ||||
| chrX:135343960-135344470 | Common:4; Rare:109 | ||||
| chrX:135344594-135344907 | Common:5; Rare:95 | ||||
| chrX:135973717-135973882 | Rare:64 | ||||
| chrX:135985232-135985508 | Rare:67; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chrX:136147308-136147577 | Common:7; Rare:71 | ||||
| chrX:136169300-136169760 | Common:4; Rare:84 | ||||
| chrX:136251354-136251514 | Rare:44 | ||||
| chrX:136497049-136497255 | Rare:48 | ||||
| chrX:136497461-136497647 | Rare:58 |