| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:135032008-135032373 | Common:1; Rare:72 | ||||
| chrX:135052118-135052307 | Common:2; Rare:52 | ||||
| chrX:135973671-135973817 | Rare:52 | ||||
| chrX:135985329-135985503 | Rare:48; Clinvar (benign):4 | ||||
| chrX:136880675-136880948 | Common:1; Rare:70 | ||||
| chrX:139205015-139205155 | Rare:25 | ||||
| chrX:140505070-140505140 | Rare:21 | ||||
| chrX:141177074-141177310 | Common:1; Rare:31 | ||||
| chrX:149938440-149938603 | Common:1; Rare:45 | ||||
| chrX:150568310-150568640 | Common:1; Rare:67 | ||||
| chrX:151397024-151397255 | Common:5; Rare:116 | ||||
| chrX:152830706-152831066 | Common:2; Rare:67 | ||||
| chrX:153599102-153599357 | Common:13; Rare:52 | ||||
| chrX:153686671-153686867 | Rare:37 | ||||
| chrX:153794323-153794684 | Common:1; Rare:110; Clinvar (benign):2 |