| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:123960350-123960705 | Rare:25 | ||||
| chrX:123961264-123961432 | Common:2; Rare:22 | ||||
| chrX:123961565-123961850 | Rare:39 | ||||
| chrX:129523207-129523641 | Common:4; Rare:106 | ||||
| chrX:129779826-129779978 | Rare:22 | ||||
| chrX:129906073-129906201 | Rare:31 | ||||
| chrX:130165703-130165927 | Rare:42; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chrX:130401884-130402035 | Common:2; Rare:45 | ||||
| chrX:132023144-132023335 | Rare:48 | ||||
| chrX:132217719-132218012 | Common:1; Rare:39 | ||||
| chrX:132218045-132218297 | Rare:29 | ||||
| chrX:132219460-132219785 | Rare:40 | ||||
| chrX:132413573-132413734 | Rare:21 | ||||
| chrX:134373141-134373480 | Common:4; Rare:70; Clinvar (benign):1 | ||||
| chrX:134796258-134796421 | Common:1; Rare:11 |