| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:38220821-38221006 | Rare:39 | ||||
| chrX:47144684-47144866 | Common:1; Rare:29 | ||||
| chrX:47483169-47483277 | Common:3; Rare:14 | ||||
| chrX:48508823-48509055 | Common:1; Rare:46 | ||||
| chrX:51893339-51893636 | Common:2; Rare:56 | ||||
| chrX:53422652-53422925 | Common:1; Rare:62 | ||||
| chrX:55000185-55000393 | Rare:40 | ||||
| chrX:56563501-56563668 | Rare:43; Clinvar:1 | ||||
| chrX:56729461-56729516 | Common:1; Rare:8 | ||||
| chrX:68498979-68499054 | Rare:16 | ||||
| chrX:70289875-70290113 | Rare:45 | ||||
| chrX:72273675-72273886 | Common:1; Rare:40 | ||||
| chrX:77895398-77895729 | Rare:95; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chrX:81201927-81202139 | Rare:38 | ||||
| chrX:100820226-100820411 | Common:2; Rare:43 |