| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:119791572-119791716 | Rare:56 | ||||
| chrX:119871683-119871921 | Common:1; Rare:56; Clinvar (benign):3 | ||||
| chrX:120630030-120630312 | Common:3; Rare:58 | ||||
| chrX:123859690-123860005 | Common:2; Rare:44 | ||||
| chrX:123961264-123961318 | Common:2; Rare:14 | ||||
| chrX:123961366-123961432 | Rare:4 | ||||
| chrX:123961525-123961806 | Rare:39 | ||||
| chrX:129843781-129844034 | Common:1; Rare:31 | ||||
| chrX:129905930-129906205 | Rare:72 | ||||
| chrX:130165697-130165954 | Rare:51; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chrX:130401898-130402035 | Common:2; Rare:42 | ||||
| chrX:132023135-132023395 | Rare:59 | ||||
| chrX:134915198-134915403 | Common:1; Rare:29 | ||||
| chrX:135032096-135032365 | Common:1; Rare:54 | ||||
| chrX:137565922-137566164 | Common:2; Rare:45 |