| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:48696573-48696761 | Rare:41 | ||||
| chrX:48911620-48911722 | Rare:26; Clinvar (benign):4 | ||||
| chrX:48958355-48958694 | Rare:61 | ||||
| chrX:49079865-49079963 | Rare:17 | ||||
| chrX:49171870-49171983 | Rare:12 | ||||
| chrX:49186371-49186596 | Common:2; Rare:36 | ||||
| chrX:49922321-49922744 | Common:1; Rare:88 | ||||
| chrX:51496530-51496690 | Common:1; Rare:38 | ||||
| chrX:51743325-51743468 | Rare:21 | ||||
| chrX:51893288-51893660 | Common:2; Rare:71 | ||||
| chrX:53225195-53225511 | Common:2; Rare:100 | ||||
| chrX:53422622-53422782 | Rare:46 | ||||
| chrX:53434341-53434487 | Common:1; Rare:34 | ||||
| chrX:53684280-53684417 | Rare:25 | ||||
| chrX:54045067-54045262 | Rare:33 |