| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:111680970-111681234 | Rare:62; Clinvar (benign):5 | ||||
| chrX:115561073-115561253 | Common:1; Rare:31 | ||||
| chrX:119236484-119236648 | Rare:51 | ||||
| chrX:119468216-119468495 | Common:3; Rare:94 | ||||
| chrX:119574373-119574619 | Rare:52 | ||||
| chrX:119791626-119791989 | Common:2; Rare:88 | ||||
| chrX:119871658-119872007 | Common:2; Rare:75; Clinvar (benign):4 | ||||
| chrX:120559891-120560207 | Rare:48 | ||||
| chrX:120560283-120560915 | Rare:114; Clinvar:5 | ||||
| chrX:120603823-120604232 | Rare:79 | ||||
| chrX:123732991-123733157 | Rare:31; Clinvar (benign):1 | ||||
| chrX:123859714-123860020 | Common:2; Rare:44 | ||||
| chrX:123961263-123961432 | Common:2; Rare:22 | ||||
| chrX:123961482-123961845 | Rare:50 | ||||
| chrX:130110526-130110644 | Rare:29 |