| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:47659115-47659246 | Rare:39 | ||||
| chrX:47836801-47836961 | Common:1; Rare:34 | ||||
| chrX:48003960-48004142 | Rare:49 | ||||
| chrX:48476135-48476230 | Rare:20 | ||||
| chrX:48508869-48508992 | Rare:19 | ||||
| chrX:48521704-48521870 | Rare:29 | ||||
| chrX:48574241-48574544 | Common:2; Rare:89 | ||||
| chrX:48574863-48574974 | Rare:33 | ||||
| chrX:48597423-48597556 | Rare:20 | ||||
| chrX:48696476-48696765 | Common:2; Rare:63 | ||||
| chrX:48911634-48911711 | Rare:19; Clinvar (benign):3 | ||||
| chrX:49002153-49002502 | Common:2; Rare:65 | ||||
| chrX:49073995-49074180 | Rare:45 | ||||
| chrX:49079857-49079960 | Rare:16 | ||||
| chrX:50814011-50814149 | Rare:32 |