| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:132219445-132219710 | Rare:25 | ||||
| chrX:134373180-134373383 | Common:4; Rare:49 | ||||
| chrX:135022468-135022560 | Rare:32 | ||||
| chrX:135973682-135973872 | Rare:64 | ||||
| chrX:135985327-135985505 | Rare:50; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chrX:136880675-136880890 | Common:1; Rare:54 | ||||
| chrX:139933041-139933215 | Rare:36 | ||||
| chrX:141177017-141177314 | Common:1; Rare:44 | ||||
| chrX:149540856-149541048 | Common:3; Rare:34 | ||||
| chrX:151397054-151397266 | Common:4; Rare:104 | ||||
| chrX:152830661-152831116 | Common:5; Rare:87 | ||||
| chrX:152941534-152941709 | Common:1; Rare:41 | ||||
| chrX:153494726-153495005 | Common:3; Rare:41 | ||||
| chrX:153599087-153599363 | Common:13; Rare:54 | ||||
| chrX:153794313-153794690 | Common:1; Rare:116; Clinvar (benign):2 |