| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:134460074-134460303 | Common:3; Rare:65 | ||||
| chrX:134797139-134797404 | Rare:44 | ||||
| chrX:134915198-134915370 | Common:1; Rare:21 | ||||
| chrX:135344698-135344812 | Rare:18 | ||||
| chrX:135520510-135520806 | Rare:47 | ||||
| chrX:135973720-135973786 | Rare:19 | ||||
| chrX:135985342-135985505 | Rare:48; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chrX:136497076-136497425 | Common:3; Rare:89 | ||||
| chrX:136880688-136880912 | Common:1; Rare:52 | ||||
| chrX:149504378-149504474 | Rare:13 | ||||
| chrX:149505245-149505409 | Rare:49 | ||||
| chrX:149540817-149541059 | Common:4; Rare:45 | ||||
| chrX:149631731-149631859 | Common:1; Rare:27 | ||||
| chrX:149938417-149938667 | Common:2; Rare:63 | ||||
| chrX:150568298-150568640 | Common:1; Rare:71 |