| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:119606422-119606602 | Common:1; Rare:35 | ||||
| chrX:120015534-120015626 | Common:5; Rare:10 | ||||
| chrX:120137052-120137220 | Common:3; Rare:17 | ||||
| chrX:120245177-120245216 | Rare:4 | ||||
| chrX:125204302-125204527 | Rare:25 | ||||
| chrX:126472546-126472616 | Common:1; Rare:10 | ||||
| chrX:134549630-134549798 | Common:1; Rare:42 | ||||
| chrX:134803652-134803803 | Common:1; Rare:17 | ||||
| chrX:136936273-136936435 | Rare:18 | ||||
| chrX:149940059-149940138 | Common:1; Rare:17 | ||||
| chrX:153381953-153382183 | Rare:26 | ||||
| chrX:153411274-153411521 | Common:2; Rare:65 | ||||
| chrX:153413997-153414137 | Common:1; Rare:16 | ||||
| chrX:154366044-154366430 | Common:3; Rare:125; Clinvar:14; Clinvar (benign):16 |