| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:153687757-153687940 | Common:4; Rare:17 | ||||
| chrX:153724346-153724469 | Common:1; Rare:32 | ||||
| chrX:153724660-153724857 | Common:1; Rare:39 | ||||
| chrX:153794324-153794697 | Common:1; Rare:117; Clinvar (benign):2 | ||||
| chrX:153829046-153829715 | Rare:149 | ||||
| chrX:153830874-153831132 | Common:1; Rare:32 | ||||
| chrX:153886126-153886322 | Common:1; Rare:34 | ||||
| chrX:153928246-153928688 | Common:4; Rare:73 | ||||
| chrX:153934928-153935328 | Common:2; Rare:140 | ||||
| chrX:153944570-153944840 | Common:2; Rare:57 | ||||
| chrX:153971182-153971365 | Rare:43 | ||||
| chrX:153971802-153971944 | Rare:41 | ||||
| chrX:153972106-153972295 | Rare:53 | ||||
| chrX:153972606-153973041 | Common:4; Rare:116 | ||||
| chrX:154019750-154020080 | Rare:72 |