| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:53686317-53686440 | Rare:20 | ||||
| chrX:54043931-54044053 | Rare:23 | ||||
| chrX:54530064-54530252 | Common:2; Rare:25 | ||||
| chrX:55000183-55000415 | Rare:51 | ||||
| chrX:55161097-55161239 | Rare:43 | ||||
| chrX:68498970-68499049 | Rare:19 | ||||
| chrX:70289879-70290130 | Rare:47 | ||||
| chrX:77895417-77895750 | Rare:90; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chrX:81201884-81202150 | Rare:43 | ||||
| chrX:101390783-101391050 | Rare:72 | ||||
| chrX:101407799-101408274 | Common:5; Rare:86; Clinvar:2; Clinvar (benign):11 | ||||
| chrX:103214974-103215155 | Common:2; Rare:40 | ||||
| chrX:103629451-103629527 | Rare:18 | ||||
| chrX:104156955-104157063 | Common:1; Rare:18 | ||||
| chrX:108091504-108091818 | Rare:85 |