| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:151397023-151397286 | Common:9; Rare:249 | ||||
| chrX:151974627-151974821 | Common:1; Rare:119 | ||||
| chrX:152830706-152831104 | Common:4; Rare:138 | ||||
| chrX:152941500-152941701 | Common:2; Rare:95 | ||||
| chrX:153333984-153334215 | Common:1; Rare:64 | ||||
| chrX:153599090-153599495 | Common:32; Rare:162 | ||||
| chrX:153687761-153687938 | Common:4; Rare:27 | ||||
| chrX:153723789-153724152 | Common:5; Rare:115 | ||||
| chrX:153724329-153724639 | Common:3; Rare:120 | ||||
| chrX:153724548-153724906 | Common:2; Rare:113 | ||||
| chrX:153725732-153725851 | Rare:34; Clinvar (benign):1 | ||||
| chrX:153725970-153726450 | Common:3; Rare:160; Clinvar:9; Clinvar (pathogenic):1 | ||||
| chrX:153764031-153764249 | Common:1; Rare:48 | ||||
| chrX:153787840-153788240 | Common:3; Rare:124 | ||||
| chrX:153794014-153794171 | Common:2; Rare:42 |