| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:46836717-46837090 | Rare:69; Clinvar:3; Clinvar (benign):1 | ||||
| chrX:46912249-46912316 | Rare:12 | ||||
| chrX:47144474-47144837 | Common:2; Rare:79; Clinvar (benign):1 | ||||
| chrX:47145090-47145311 | Rare:32 | ||||
| chrX:47482548-47482665 | Common:5; Rare:26; Clinvar:2 | ||||
| chrX:47482928-47483029 | Rare:18 | ||||
| chrX:47483159-47483277 | Common:3; Rare:17 | ||||
| chrX:47561115-47561227 | Rare:18 | ||||
| chrX:47659057-47659235 | Rare:51 | ||||
| chrX:47836791-47836953 | Common:1; Rare:38 | ||||
| chrX:48003960-48004122 | Rare:43 | ||||
| chrX:48468298-48468491 | Common:1; Rare:25 | ||||
| chrX:48469350-48469622 | Rare:40 | ||||
| chrX:48470180-48470380 | Common:1; Rare:28 | ||||
| chrX:48475880-48476343 | Rare:76 |