| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:76172797-76173163 | Rare:72 | ||||
| chrX:77895395-77895750 | Rare:102; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chrX:77899233-77899565 | Common:1; Rare:80; Clinvar:1; Clinvar (benign):1 | ||||
| chrX:77910487-77910815 | Common:1; Rare:47 | ||||
| chrX:78064949-78065219 | Common:1; Rare:37 | ||||
| chrX:78103927-78104380 | Common:4; Rare:165 | ||||
| chrX:78139609-78139745 | Common:2; Rare:63 | ||||
| chrX:79367260-79367410 | Common:1; Rare:24 | ||||
| chrX:80335269-80335490 | Common:2; Rare:59 | ||||
| chrX:80809783-80810186 | Common:1; Rare:51 | ||||
| chrX:81121618-81121863 | Common:2; Rare:38 | ||||
| chrX:81201706-81201824 | Rare:9 | ||||
| chrX:81201876-81202222 | Rare:57 | ||||
| chrX:85003738-85003909 | Common:2; Rare:32 | ||||
| chrX:85243891-85244163 | Common:1; Rare:65; Clinvar (benign):1 |