| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:111681148-111681298 | Rare:48; Clinvar (benign):7 | ||||
| chrX:112840868-112841055 | Rare:33 | ||||
| chrX:118345867-118346185 | Common:3; Rare:57 | ||||
| chrX:119236581-119236651 | Rare:19 | ||||
| chrX:119468216-119468506 | Common:3; Rare:97 | ||||
| chrX:119574373-119574619 | Rare:52 | ||||
| chrX:119791596-119791958 | Common:2; Rare:94 | ||||
| chrX:119871621-119871904 | Common:2; Rare:59; Clinvar (benign):2 | ||||
| chrX:120560748-120560859 | Rare:14 | ||||
| chrX:120604061-120604150 | Rare:21 | ||||
| chrX:120630030-120630168 | Rare:31 | ||||
| chrX:123184136-123184414 | Rare:40 | ||||
| chrX:123859690-123860042 | Common:2; Rare:51 | ||||
| chrX:123860045-123860188 | Rare:24 | ||||
| chrX:123960350-123960732 | Rare:28 |