| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:71254082-71254238 | Common:2; Rare:27 | ||||
| chrX:71254677-71254805 | Common:1; Rare:12 | ||||
| chrX:71255247-71255324 | Rare:13 | ||||
| chrX:71283347-71283731 | Rare:58 | ||||
| chrX:71365864-71366266 | Common:4; Rare:76 | ||||
| chrX:71366494-71366583 | Common:3; Rare:31 | ||||
| chrX:71532882-71533161 | Rare:55 | ||||
| chrX:72181297-72181324 | Rare:7 | ||||
| chrX:72181532-72181798 | Common:2; Rare:68 | ||||
| chrX:72238936-72239166 | Common:4; Rare:71 | ||||
| chrX:72714054-72714439 | Common:2; Rare:70; Clinvar (benign):1 | ||||
| chrX:73214797-73215009 | Common:1; Rare:25 | ||||
| chrX:73562846-73563527 | Common:1; Rare:152 | ||||
| chrX:74614422-74614835 | Common:1; Rare:90 | ||||
| chrX:75156239-75156378 | Common:2; Rare:41 |