| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:20267003-20267295 | Common:1; Rare:50 | ||||
| chrX:21374096-21374477 | Common:4; Rare:89 | ||||
| chrX:21940461-21940858 | Common:2; Rare:96 | ||||
| chrX:23743156-23743398 | Common:5; Rare:47 | ||||
| chrX:23782984-23783423 | Common:5; Rare:99 | ||||
| chrX:23783541-23783738 | Common:2; Rare:47 | ||||
| chrX:23784950-23785560 | Common:2; Rare:111 | ||||
| chrX:23907698-23908006 | Common:1; Rare:65 | ||||
| chrX:24054670-24054987 | Rare:70 | ||||
| chrX:24149611-24149778 | Rare:30 | ||||
| chrX:24465022-24465329 | Common:4; Rare:84 | ||||
| chrX:30653106-30653532 | Common:2; Rare:111 | ||||
| chrX:33211464-33211689 | Rare:43; Clinvar:3; Clinvar (benign):1 | ||||
| chrX:37349073-37349398 | Common:2; Rare:46 | ||||
| chrX:37847513-37847631 | Rare:32 |