| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:135344632-135344814 | Common:1; Rare:32 | ||||
| chrX:135973717-135973842 | Rare:44 | ||||
| chrX:135973980-135974001 | Rare:4 | ||||
| chrX:141177070-141177314 | Common:1; Rare:31 | ||||
| chrX:149505282-149505398 | Rare:27 | ||||
| chrX:151974674-151974964 | Common:1; Rare:77 | ||||
| chrX:152830706-152831038 | Common:1; Rare:62 | ||||
| chrX:153794330-153794682 | Common:1; Rare:109; Clinvar (benign):2 | ||||
| chrX:154428457-154428695 | Common:2; Rare:41 | ||||
| chrX:154516165-154516536 | Common:4; Rare:77 | ||||
| chrX:154547550-154547639 | Common:1; Rare:24; Clinvar (benign):1 |