| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:71532894-71533146 | Rare:49 | ||||
| chrX:77895400-77895750 | Rare:99; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chrX:78103974-78104289 | Common:4; Rare:106 | ||||
| chrX:78139583-78139804 | Common:2; Rare:92 | ||||
| chrX:81201884-81202159 | Rare:45 | ||||
| chrX:100820220-100820417 | Common:2; Rare:46 | ||||
| chrX:101348711-101348822 | Common:2; Rare:16 | ||||
| chrX:101407893-101408274 | Common:5; Rare:71; Clinvar:1; Clinvar (benign):10 | ||||
| chrX:104156902-104157070 | Common:1; Rare:28 | ||||
| chrX:108091511-108091829 | Rare:84 | ||||
| chrX:110318072-110318249 | Rare:45 | ||||
| chrX:118345861-118346171 | Common:3; Rare:54 | ||||
| chrX:118975282-118975381 | Rare:23 | ||||
| chrX:119791596-119791714 | Rare:47 | ||||
| chrX:119871687-119871909 | Common:1; Rare:56; Clinvar (benign):3 |