| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:51496559-51496956 | Common:2; Rare:95 | ||||
| chrX:51803014-51803109 | Rare:23 | ||||
| chrX:53422645-53422918 | Common:1; Rare:64 | ||||
| chrX:53434356-53434477 | Common:1; Rare:26 | ||||
| chrX:53686307-53686512 | Rare:38 | ||||
| chrX:53686586-53686680 | Common:3; Rare:22 | ||||
| chrX:54357844-54358146 | Rare:57 | ||||
| chrX:54440240-54440464 | Rare:44 | ||||
| chrX:54530046-54530301 | Common:2; Rare:36 | ||||
| chrX:55000195-55000390 | Rare:38 | ||||
| chrX:55161097-55161276 | Rare:54 | ||||
| chrX:56232286-56232443 | Rare:23 | ||||
| chrX:56563811-56564176 | Common:1; Rare:85; Clinvar (benign):1 | ||||
| chrX:56995500-56995632 | Common:1; Rare:26 | ||||
| chrX:57121472-57121578 | Common:1; Rare:20 |