| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:78104047-78104310 | Common:4; Rare:99 | ||||
| chrX:81201911-81202189 | Rare:50 | ||||
| chrX:101390818-101391050 | Rare:67 | ||||
| chrX:101407841-101408292 | Common:5; Rare:85; Clinvar:2; Clinvar (benign):11 | ||||
| chrX:103356165-103356603 | Common:4; Rare:58 | ||||
| chrX:104156966-104157069 | Common:1; Rare:17 | ||||
| chrX:108091516-108091818 | Rare:80 | ||||
| chrX:110318077-110318258 | Rare:45 | ||||
| chrX:119468253-119468506 | Common:3; Rare:89 | ||||
| chrX:119574384-119574586 | Rare:43 | ||||
| chrX:119791596-119791978 | Common:2; Rare:100 | ||||
| chrX:119871687-119871914 | Common:1; Rare:56; Clinvar (benign):3 | ||||
| chrX:120559865-120560114 | Rare:39 | ||||
| chrX:120604052-120604152 | Rare:22 | ||||
| chrX:120629938-120630309 | Common:4; Rare:72 |