| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:111680984-111681299 | Rare:79; Clinvar (benign):7 | ||||
| chrX:118116705-118116882 | Common:1; Rare:28 | ||||
| chrX:119399017-119399346 | Common:3; Rare:63 | ||||
| chrX:119468191-119468497 | Common:3; Rare:101 | ||||
| chrX:119469075-119469279 | Rare:60 | ||||
| chrX:119574364-119574575 | Rare:48 | ||||
| chrX:119758426-119758591 | Common:2; Rare:27 | ||||
| chrX:119791626-119791735 | Common:1; Rare:40 | ||||
| chrX:119871648-119871891 | Common:1; Rare:51; Clinvar (benign):2 | ||||
| chrX:119943712-119943851 | Rare:25 | ||||
| chrX:120469066-120469336 | Common:1; Rare:68; Clinvar:8; Clinvar (benign):7 | ||||
| chrX:120604050-120604226 | Rare:37 | ||||
| chrX:123733025-123733187 | Rare:31 | ||||
| chrX:123961256-123961331 | Common:2; Rare:18 | ||||
| chrX:123961540-123961828 | Rare:41 |