| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:135052100-135052349 | Common:2; Rare:69 | ||||
| chrX:135344633-135344821 | Common:1; Rare:34 | ||||
| chrX:135973695-135973820 | Rare:45 | ||||
| chrX:139933025-139933198 | Rare:33 | ||||
| chrX:141177036-141177314 | Common:1; Rare:41 | ||||
| chrX:150898590-150898876 | Common:2; Rare:83 | ||||
| chrX:151396988-151397295 | Common:5; Rare:144 | ||||
| chrX:152830712-152831094 | Common:2; Rare:67 | ||||
| chrX:153599079-153599350 | Common:13; Rare:56 | ||||
| chrX:153794291-153794699 | Common:1; Rare:127; Clinvar (benign):2 | ||||
| chrX:153971173-153971278 | Rare:25 | ||||
| chrX:154371173-154371525 | Common:1; Rare:93; Clinvar:5; Clinvar (benign):8 | ||||
| chrX:154428457-154428689 | Common:2; Rare:40 | ||||
| chrX:154516179-154516531 | Common:4; Rare:74 | ||||
| chrX:154547553-154547639 | Common:1; Rare:23; Clinvar (benign):1 |