| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:47145168-47145347 | Rare:32 | ||||
| chrX:47202353-47202687 | Common:1; Rare:75; Clinvar:1; Clinvar (benign):1 | ||||
| chrX:47218646-47218776 | Rare:65 | ||||
| chrX:47222049-47222319 | Common:1; Rare:23 | ||||
| chrX:47226646-47226883 | Rare:35 | ||||
| chrX:47232789-47233219 | Rare:106 | ||||
| chrX:47482923-47483086 | Rare:32 | ||||
| chrX:47483169-47483234 | Common:1; Rare:9 | ||||
| chrX:47560995-47561239 | Common:1; Rare:43 | ||||
| chrX:47659053-47659189 | Rare:38 | ||||
| chrX:47836845-47836978 | Rare:26 | ||||
| chrX:48475892-48476253 | Rare:64 | ||||
| chrX:48508823-48509058 | Common:1; Rare:48 | ||||
| chrX:48574235-48574558 | Common:2; Rare:95 | ||||
| chrX:48574880-48575223 | Common:3; Rare:83 |