| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:48574869-48575190 | Common:3; Rare:84 | ||||
| chrX:48696587-48696777 | Rare:41 | ||||
| chrX:48801674-48802016 | Rare:66 | ||||
| chrX:48898117-48898272 | Common:1; Rare:23 | ||||
| chrX:48911626-48911715 | Rare:23; Clinvar (benign):3 | ||||
| chrX:48911932-48912155 | Common:1; Rare:37 | ||||
| chrX:48958317-48958414 | Rare:27 | ||||
| chrX:48971836-48972054 | Rare:27 | ||||
| chrX:49002186-49002265 | Rare:25 | ||||
| chrX:49039885-49040007 | Rare:18 | ||||
| chrX:49073991-49074083 | Rare:26 | ||||
| chrX:49079764-49079972 | Rare:28 | ||||
| chrX:49171775-49172103 | Common:4; Rare:53 | ||||
| chrX:49186287-49186482 | Common:1; Rare:34 | ||||
| chrX:49879396-49879624 | Rare:43 |