| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:49200179-49200348 | Rare:46; Clinvar:1 | ||||
| chrX:49879454-49879602 | Rare:29 | ||||
| chrX:51743356-51743460 | Rare:12 | ||||
| chrX:53281519-53281538 | Rare:1 | ||||
| chrX:53422616-53422920 | Common:2; Rare:82; Clinvar (benign):1 | ||||
| chrX:53536172-53536502 | Common:3; Rare:56; Clinvar (benign):1 | ||||
| chrX:54043920-54044004 | Rare:14 | ||||
| chrX:54440271-54440475 | Rare:45 | ||||
| chrX:54530043-54530309 | Common:2; Rare:38 | ||||
| chrX:55000194-55000390 | Rare:38 | ||||
| chrX:55161097-55161276 | Rare:54 | ||||
| chrX:57121414-57121618 | Common:1; Rare:48 | ||||
| chrX:63351310-63351569 | Common:2; Rare:61 | ||||
| chrX:63755065-63755324 | Rare:56 | ||||
| chrX:64205690-64205977 | Common:1; Rare:51 |