| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:153934761-153934912 | Common:1; Rare:24 | ||||
| chrX:153934956-153935342 | Common:1; Rare:92 | ||||
| chrX:153971132-153971314 | Rare:43 | ||||
| chrX:153971329-153971399 | Rare:16 | ||||
| chrX:153971795-153972027 | Rare:67 | ||||
| chrX:153972412-153972790 | Common:2; Rare:116 | ||||
| chrX:154353035-154353434 | Common:3; Rare:93; Clinvar:7; Clinvar (benign):9 | ||||
| chrX:154354446-154354678 | Common:1; Rare:44; Clinvar:1; Clinvar (benign):6 | ||||
| chrX:154397603-154397775 | Common:1; Rare:36 | ||||
| chrX:154398788-154399052 | Common:4; Rare:59 | ||||
| chrX:154409175-154409427 | Rare:39 | ||||
| chrX:154411430-154411555 | Rare:22 | ||||
| chrX:154428457-154428707 | Common:2; Rare:44 | ||||
| chrX:154478744-154479064 | Common:4; Rare:92 | ||||
| chrX:154479211-154479344 | Rare:28 |