| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:118974566-118974645 | Rare:15 | ||||
| chrX:118975218-118975426 | Rare:43 | ||||
| chrX:119236551-119236691 | Rare:35 | ||||
| chrX:119468209-119468524 | Common:3; Rare:103 | ||||
| chrX:119469064-119469205 | Rare:39 | ||||
| chrX:119574356-119574613 | Rare:55 | ||||
| chrX:119791553-119791994 | Common:2; Rare:115 | ||||
| chrX:119871605-119871969 | Common:2; Rare:71; Clinvar (benign):3 | ||||
| chrX:119943574-119943852 | Rare:54 | ||||
| chrX:120560910-120561124 | Rare:45 | ||||
| chrX:120603987-120604049 | Rare:7 | ||||
| chrX:120604052-120604158 | Rare:24 | ||||
| chrX:120629916-120630312 | Common:4; Rare:75 | ||||
| chrX:123859684-123860170 | Common:2; Rare:74 | ||||
| chrX:123961540-123961835 | Rare:42 |