| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:118974506-118974645 | Rare:26 | ||||
| chrX:118975132-118975426 | Common:2; Rare:85 | ||||
| chrX:119468238-119468506 | Common:3; Rare:93 | ||||
| chrX:119469043-119469284 | Rare:67 | ||||
| chrX:119574364-119574755 | Common:1; Rare:78 | ||||
| chrX:119791581-119791994 | Common:2; Rare:111 | ||||
| chrX:119852915-119853226 | Common:3; Rare:50; Clinvar (benign):3 | ||||
| chrX:119871614-119871992 | Common:2; Rare:75; Clinvar (benign):3 | ||||
| chrX:120560722-120560860 | Rare:20 | ||||
| chrX:120560929-120561119 | Rare:37 | ||||
| chrX:120561404-120561592 | Common:1; Rare:33 | ||||
| chrX:120629916-120630266 | Common:4; Rare:67 | ||||
| chrX:123733018-123733086 | Rare:14 | ||||
| chrX:123859938-123860266 | Rare:60 | ||||
| chrX:123960270-123960563 | Rare:34 |