| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:136497368-136497647 | Common:1; Rare:58 | ||||
| chrX:139932992-139933169 | Rare:30 | ||||
| chrX:141176472-141176558 | Rare:23 | ||||
| chrX:141177036-141177320 | Common:1; Rare:43 | ||||
| chrX:149540417-149540663 | Common:2; Rare:26 | ||||
| chrX:149540766-149541211 | Common:6; Rare:73 | ||||
| chrX:149938396-149938677 | Common:2; Rare:72 | ||||
| chrX:151396874-151397341 | Common:7; Rare:195; Clinvar:1; Clinvar (benign):1 | ||||
| chrX:152830708-152831116 | Common:2; Rare:72 | ||||
| chrX:152941554-152941711 | Common:1; Rare:38 | ||||
| chrX:153494703-153495062 | Common:3; Rare:59 | ||||
| chrX:153495429-153495596 | Rare:26 | ||||
| chrX:153599043-153599363 | Common:15; Rare:61 | ||||
| chrX:153723840-153724162 | Common:4; Rare:60 | ||||
| chrX:153724329-153724537 | Common:2; Rare:57 |