| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:48521791-48521876 | Rare:15 | ||||
| chrX:48574853-48575240 | Common:3; Rare:94 | ||||
| chrX:48761431-48761820 | Common:3; Rare:49 | ||||
| chrX:48761869-48761914 | Rare:8 | ||||
| chrX:48802760-48802918 | Rare:28 | ||||
| chrX:48911613-48911715 | Rare:27; Clinvar (benign):4 | ||||
| chrX:48919019-48919297 | Rare:43 | ||||
| chrX:48958302-48958555 | Rare:66 | ||||
| chrX:49002193-49002264 | Rare:23 | ||||
| chrX:49079784-49079918 | Rare:19 | ||||
| chrX:49171753-49172019 | Common:4; Rare:35 | ||||
| chrX:53082886-53082984 | Rare:33 | ||||
| chrX:53422627-53422900 | Common:1; Rare:73 | ||||
| chrX:53434356-53434469 | Common:1; Rare:26 | ||||
| chrX:54043901-54044053 | Rare:32 |