| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:120603903-120604154 | Rare:50 | ||||
| chrX:120604628-120604805 | Rare:20 | ||||
| chrX:120629905-120630312 | Common:4; Rare:75 | ||||
| chrX:123733018-123733174 | Rare:29 | ||||
| chrX:123859638-123859905 | Common:2; Rare:39 | ||||
| chrX:123960350-123960743 | Rare:28 | ||||
| chrX:123961264-123961432 | Common:2; Rare:22 | ||||
| chrX:123961540-123961834 | Rare:42 | ||||
| chrX:129779826-129779978 | Rare:22 | ||||
| chrX:129905932-129906217 | Rare:73 | ||||
| chrX:130165642-130165927 | Rare:57; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chrX:130401873-130402025 | Common:2; Rare:46 | ||||
| chrX:132023145-132023407 | Rare:61 | ||||
| chrX:132219439-132219611 | Rare:21 | ||||
| chrX:132488877-132488973 | Rare:28 |