| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:123961554-123961834 | Rare:41 | ||||
| chrX:124346461-124346574 | Rare:8; Clinvar (benign):2 | ||||
| chrX:129779826-129779980 | Rare:22 | ||||
| chrX:129843694-129844086 | Common:1; Rare:51 | ||||
| chrX:129905966-129906201 | Rare:62 | ||||
| chrX:130110405-130110623 | Rare:50 | ||||
| chrX:130165688-130165985 | Rare:64; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chrX:130171916-130171992 | Common:1; Rare:25 | ||||
| chrX:132023128-132023345 | Rare:51 | ||||
| chrX:132217719-132218012 | Common:1; Rare:39 | ||||
| chrX:132218193-132218287 | Rare:22 | ||||
| chrX:132219427-132219627 | Rare:22 | ||||
| chrX:132488917-132488985 | Rare:22 | ||||
| chrX:132489888-132490025 | Common:1; Rare:28 | ||||
| chrX:133985506-133985935 | Rare:84 |