| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:55452009-55452218 | Rare:34 | ||||
| chrX:56729452-56729525 | Common:1; Rare:9 | ||||
| chrX:57121446-57121616 | Common:1; Rare:41 | ||||
| chrX:63351310-63351567 | Common:2; Rare:61 | ||||
| chrX:65034698-65034859 | Common:1; Rare:33 | ||||
| chrX:68433331-68433437 | Rare:14 | ||||
| chrX:68433455-68433614 | Rare:32 | ||||
| chrX:68498977-68499078 | Rare:23 | ||||
| chrX:68693514-68693654 | Rare:31 | ||||
| chrX:68828837-68829025 | Rare:38 | ||||
| chrX:70289888-70290122 | Rare:43 | ||||
| chrX:71136075-71136371 | Common:2; Rare:40; Clinvar (benign):3 | ||||
| chrX:71283428-71283720 | Rare:46 | ||||
| chrX:71296848-71297182 | Rare:44 | ||||
| chrX:71532970-71533213 | Rare:45 |