| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:53422613-53422976 | Common:2; Rare:88; Clinvar (benign):1 | ||||
| chrX:53434352-53434471 | Common:1; Rare:28 | ||||
| chrX:53683788-53683951 | Common:1; Rare:31 | ||||
| chrX:53683956-53684265 | Rare:83 | ||||
| chrX:53686442-53686647 | Common:1; Rare:43 | ||||
| chrX:53686688-53686795 | Common:1; Rare:21 | ||||
| chrX:54042762-54042987 | Rare:34; Clinvar:1 | ||||
| chrX:54043116-54043250 | Rare:18 | ||||
| chrX:54043903-54044071 | Rare:33 | ||||
| chrX:54044246-54044626 | Common:1; Rare:79 | ||||
| chrX:54044951-54045026 | Rare:10 | ||||
| chrX:54045068-54045366 | Rare:47 | ||||
| chrX:54357484-54357619 | Rare:18 | ||||
| chrX:54357805-54358237 | Common:1; Rare:83 | ||||
| chrX:54440271-54440481 | Rare:49 |