| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:40097982-40098095 | Rare:12 | ||||
| chrX:45824425-45824545 | Rare:18 | ||||
| chrX:45850163-45850248 | Common:8; Rare:16 | ||||
| chrX:45850852-45850914 | Rare:12 | ||||
| chrX:46262150-46262356 | Common:2; Rare:36 | ||||
| chrX:47210663-47210911 | Common:2; Rare:30; Clinvar (benign):1 | ||||
| chrX:49173126-49173482 | Rare:82 | ||||
| chrX:53431032-53431292 | Rare:25 | ||||
| chrX:55908044-55908294 | Rare:43 | ||||
| chrX:56564717-56564766 | Rare:11 | ||||
| chrX:56810551-56810787 | Rare:23 | ||||
| chrX:65921371-65921588 | Common:1; Rare:40 | ||||
| chrX:66015249-66015458 | Common:2; Rare:33 | ||||
| chrX:66018684-66018960 | Rare:51 | ||||
| chrX:70453437-70453703 | Common:2; Rare:36 |