| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:132022949-132023336 | Rare:82 | ||||
| chrX:132218172-132218282 | Rare:21 | ||||
| chrX:134806881-134807196 | Common:1; Rare:46 | ||||
| chrX:134915198-134915422 | Common:1; Rare:33 | ||||
| chrX:135032107-135032380 | Common:1; Rare:58 | ||||
| chrX:135052083-135052369 | Common:2; Rare:81 | ||||
| chrX:135344615-135344821 | Common:1; Rare:39 | ||||
| chrX:135973702-135973777 | Rare:24 | ||||
| chrX:136147263-136147566 | Common:3; Rare:36 | ||||
| chrX:139933025-139933219 | Rare:40 | ||||
| chrX:141177008-141177325 | Common:1; Rare:48 | ||||
| chrX:149540811-149541048 | Common:4; Rare:45 | ||||
| chrX:149938434-149938660 | Common:2; Rare:57 | ||||
| chrX:150568322-150568653 | Common:1; Rare:69; Clinvar (benign):1 | ||||
| chrX:150898576-150898911 | Common:3; Rare:93 |