| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:45770135-45770417 | Rare:21 | ||||
| chrX:70435255-70435388 | Rare:10 | ||||
| chrX:73988795-73989067 | Common:1; Rare:33 | ||||
| chrX:74268359-74268433 | Rare:4 | ||||
| chrX:74292497-74292747 | Rare:45 | ||||
| chrX:74420545-74420939 | Common:2; Rare:98 | ||||
| chrX:107676972-107677165 | Rare:22 | ||||
| chrX:109732236-109732438 | Rare:37 | ||||
| chrX:115571228-115571472 | Rare:38 | ||||
| chrX:135032965-135033003 | Rare:9 | ||||
| chrX:136209766-136209966 | Common:3; Rare:58; Clinvar:2; Clinvar (benign):13 | ||||
| chrX:140783150-140783760 | Common:3; Rare:106 | ||||
| chrX:153487567-153487852 | Common:3; Rare:29 | ||||
| chrX:153496365-153496497 | Common:1; Rare:18 | ||||
| chrX:153501585-153501688 | Rare:13 |