| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:118345861-118346156 | Common:3; Rare:50 | ||||
| chrX:119468205-119468545 | Common:3; Rare:108 | ||||
| chrX:119574364-119574581 | Rare:50 | ||||
| chrX:119791584-119791978 | Common:2; Rare:107 | ||||
| chrX:119852915-119853276 | Common:3; Rare:58; Clinvar (benign):3 | ||||
| chrX:119871665-119871974 | Common:1; Rare:66; Clinvar (benign):3 | ||||
| chrX:120630008-120630324 | Common:3; Rare:63 | ||||
| chrX:123733018-123733083 | Rare:14 | ||||
| chrX:123859636-123859840 | Common:1; Rare:27 | ||||
| chrX:123961230-123961432 | Common:2; Rare:28 | ||||
| chrX:123961540-123961812 | Rare:39 | ||||
| chrX:129523296-129523618 | Common:4; Rare:75 | ||||
| chrX:129905981-129906213 | Rare:62 | ||||
| chrX:130165652-130165903 | Rare:50; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chrX:130401873-130402017 | Common:2; Rare:42 |