| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:74614440-74614820 | Common:1; Rare:84 | ||||
| chrX:75156239-75156377 | Common:2; Rare:41 | ||||
| chrX:75274495-75274706 | Common:2; Rare:46 | ||||
| chrX:75523009-75523198 | Common:1; Rare:39 | ||||
| chrX:75523239-75523423 | Common:1; Rare:28 | ||||
| chrX:77895412-77895745 | Rare:92; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chrX:78103962-78104320 | Common:4; Rare:131 | ||||
| chrX:79367108-79367454 | Common:1; Rare:64 | ||||
| chrX:81201876-81202250 | Rare:62 | ||||
| chrX:81202312-81202666 | Common:2; Rare:48 | ||||
| chrX:85243770-85243839 | Common:1; Rare:13 | ||||
| chrX:100643974-100644230 | Rare:38 | ||||
| chrX:101407845-101408292 | Common:5; Rare:84; Clinvar:2; Clinvar (benign):11 | ||||
| chrX:101485268-101485542 | Rare:40 | ||||
| chrX:102651303-102651577 | Common:2; Rare:73 |