| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:55000241-55000390 | Rare:34 | ||||
| chrX:55161097-55161239 | Rare:43 | ||||
| chrX:57121440-57121599 | Common:1; Rare:38 | ||||
| chrX:64205667-64206031 | Common:1; Rare:68 | ||||
| chrX:65034729-65034793 | Common:1; Rare:11 | ||||
| chrX:68498965-68499057 | Rare:22 | ||||
| chrX:68693465-68693732 | Rare:64 | ||||
| chrX:70289875-70290073 | Rare:41 | ||||
| chrX:71254677-71254797 | Common:1; Rare:12 | ||||
| chrX:75156018-75156067 | Common:1; Rare:10 | ||||
| chrX:75156273-75156369 | Common:2; Rare:26 | ||||
| chrX:75523015-75523149 | Rare:30 | ||||
| chrX:77895412-77895736 | Rare:89; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chrX:78104006-78104343 | Common:4; Rare:125 | ||||
| chrX:79367531-79367845 | Common:1; Rare:56 |