| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:47483169-47483261 | Common:2; Rare:14 | ||||
| chrX:47659066-47659235 | Rare:50 | ||||
| chrX:47836791-47836953 | Common:1; Rare:38 | ||||
| chrX:48003984-48004281 | Common:3; Rare:73 | ||||
| chrX:48475966-48476247 | Rare:51 | ||||
| chrX:48574885-48574956 | Rare:21 | ||||
| chrX:48911637-48911711 | Rare:17; Clinvar (benign):3 | ||||
| chrX:49079854-49079946 | Rare:15 | ||||
| chrX:49123723-49123988 | Rare:55 | ||||
| chrX:53281572-53281756 | Common:1; Rare:23 | ||||
| chrX:53422627-53422944 | Common:1; Rare:76 | ||||
| chrX:53434346-53434482 | Common:1; Rare:30 | ||||
| chrX:54440250-54440489 | Rare:51 | ||||
| chrX:55000204-55000390 | Rare:37 | ||||
| chrX:55161108-55161225 | Rare:36 |