| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:55161108-55161269 | Rare:45 | ||||
| chrX:57121476-57121557 | Common:1; Rare:18 | ||||
| chrX:65034698-65034816 | Common:1; Rare:25 | ||||
| chrX:68498961-68499056 | Rare:22 | ||||
| chrX:70289888-70290112 | Rare:40 | ||||
| chrX:71532971-71533136 | Rare:29 | ||||
| chrX:75156277-75156315 | Common:1; Rare:9 | ||||
| chrX:77895403-77895731 | Rare:90; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chrX:81201876-81202197 | Rare:53 | ||||
| chrX:101407872-101408274 | Common:5; Rare:75; Clinvar:1; Clinvar (benign):10 | ||||
| chrX:103585455-103585655 | Common:3; Rare:43 | ||||
| chrX:103586476-103586807 | Rare:69 | ||||
| chrX:104156955-104157063 | Common:1; Rare:18 | ||||
| chrX:107717044-107717181 | Rare:23 | ||||
| chrX:108091504-108091822 | Rare:86 |