| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:131289237-131289480 | Common:2; Rare:61 | ||||
| chrX:132023108-132023345 | Rare:54 | ||||
| chrX:132218030-132218239 | Rare:13 | ||||
| chrX:134373143-134373447 | Common:4; Rare:64 | ||||
| chrX:135052114-135052279 | Common:1; Rare:44 | ||||
| chrX:135344626-135344812 | Common:1; Rare:34 | ||||
| chrX:135973704-135973772 | Rare:22 | ||||
| chrX:135985305-135985510 | Rare:56; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chrX:136497128-136497404 | Common:3; Rare:75 | ||||
| chrX:136880604-136880951 | Common:1; Rare:84 | ||||
| chrX:137565859-137566164 | Common:2; Rare:59 | ||||
| chrX:138711652-138711917 | Common:2; Rare:50 | ||||
| chrX:139933025-139933266 | Rare:42 | ||||
| chrX:141177030-141177368 | Common:2; Rare:55 | ||||
| chrX:149938440-149938632 | Common:1; Rare:50 |