| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:30308591-30308705 | Rare:27; Clinvar (pathogenic):1 | ||||
| chrX:38220815-38220995 | Rare:39 | ||||
| chrX:40647525-40647758 | Common:4; Rare:80 | ||||
| chrX:46545413-46545531 | Rare:22 | ||||
| chrX:47659103-47659267 | Rare:47 | ||||
| chrX:48508879-48509036 | Rare:30 | ||||
| chrX:49002227-49002265 | Rare:15 | ||||
| chrX:49269613-49269846 | Rare:45 | ||||
| chrX:53422645-53422933 | Common:1; Rare:64 | ||||
| chrX:56563473-56563665 | Rare:45; Clinvar:1 | ||||
| chrX:57121422-57121597 | Common:1; Rare:41 | ||||
| chrX:57121615-57121678 | Rare:14 | ||||
| chrX:63351295-63351464 | Common:1; Rare:46 | ||||
| chrX:65034708-65034826 | Common:1; Rare:25 | ||||
| chrX:68498960-68499058 | Rare:22 |