| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:13734576-13734859 | Common:3; Rare:85; Clinvar (benign):1 | ||||
| chrX:16719442-16719690 | Rare:72 | ||||
| chrX:16786219-16786498 | Common:1; Rare:58 | ||||
| chrX:19670887-19671148 | Common:1; Rare:43 | ||||
| chrX:20267064-20267281 | Common:1; Rare:38 | ||||
| chrX:23907873-23908068 | Rare:40 | ||||
| chrX:47144668-47144794 | Rare:23 | ||||
| chrX:47145089-47145269 | Rare:28 | ||||
| chrX:47232920-47233026 | Rare:27 | ||||
| chrX:48521675-48521882 | Rare:36 | ||||
| chrX:48911640-48911737 | Rare:21; Clinvar (benign):3 | ||||
| chrX:53422613-53422920 | Common:2; Rare:82; Clinvar (benign):1 | ||||
| chrX:54530047-54530252 | Common:2; Rare:28 | ||||
| chrX:55000204-55000381 | Rare:32 | ||||
| chrX:68498965-68499059 | Rare:22 |