| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:123732996-123733189 | Rare:37; Clinvar (benign):1 | ||||
| chrX:123960350-123960705 | Rare:25 | ||||
| chrX:123961269-123961432 | Common:2; Rare:22 | ||||
| chrX:123961957-123962088 | Rare:18 | ||||
| chrX:129779792-129779989 | Rare:32 | ||||
| chrX:129843795-129844069 | Common:1; Rare:36 | ||||
| chrX:129906031-129906198 | Rare:45 | ||||
| chrX:130165735-130165987 | Rare:51; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chrX:130339786-130339970 | Rare:27 | ||||
| chrX:130401898-130402015 | Common:2; Rare:35 | ||||
| chrX:132023160-132023345 | Rare:45 | ||||
| chrX:132218068-132218239 | Rare:10 | ||||
| chrX:132489001-132489173 | Rare:29 | ||||
| chrX:132489918-132490204 | Common:1; Rare:50 | ||||
| chrX:134373141-134373429 | Common:4; Rare:63 |