| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:24054905-24054987 | Rare:30 | ||||
| chrX:37847506-37847642 | Rare:35 | ||||
| chrX:40580754-40581021 | Common:4; Rare:67; Clinvar (benign):1 | ||||
| chrX:46545385-46545540 | Rare:31 | ||||
| chrX:47144659-47144843 | Common:1; Rare:29 | ||||
| chrX:47145097-47145309 | Rare:32 | ||||
| chrX:47233301-47233456 | Rare:26 | ||||
| chrX:47482586-47482665 | Common:5; Rare:18; Clinvar:2 | ||||
| chrX:47483159-47483277 | Common:3; Rare:17 | ||||
| chrX:48919013-48919265 | Rare:40 | ||||
| chrX:49079837-49079937 | Rare:13 | ||||
| chrX:49186371-49186504 | Common:1; Rare:24 | ||||
| chrX:49200179-49200363 | Rare:50; Clinvar:1 | ||||
| chrX:53082112-53082367 | Common:1; Rare:61 | ||||
| chrX:53422632-53422971 | Common:1; Rare:76 |