| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:70289858-70290104 | Rare:43 | ||||
| chrX:71283383-71283719 | Rare:55 | ||||
| chrX:75156250-75156369 | Common:2; Rare:36 | ||||
| chrX:75274610-75274717 | Common:2; Rare:22 | ||||
| chrX:77895396-77895744 | Rare:100; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chrX:81201884-81202219 | Rare:55 | ||||
| chrX:101407905-101408285 | Common:5; Rare:69; Clinvar (benign):9 | ||||
| chrX:101623019-101623201 | Rare:36 | ||||
| chrX:103356267-103356572 | Common:3; Rare:45 | ||||
| chrX:103376452-103376598 | Common:1; Rare:23 | ||||
| chrX:103686684-103686995 | Common:4; Rare:39 | ||||
| chrX:104156942-104157069 | Common:1; Rare:22 | ||||
| chrX:108091457-108091818 | Rare:95 | ||||
| chrX:119236050-119236365 | Rare:81 | ||||
| chrX:119398996-119399368 | Common:3; Rare:69 |