| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:75156012-75156067 | Common:1; Rare:13 | ||||
| chrX:75156229-75156370 | Common:2; Rare:43 | ||||
| chrX:75523018-75523144 | Rare:28 | ||||
| chrX:75523257-75523546 | Common:3; Rare:41 | ||||
| chrX:76172958-76173154 | Rare:49 | ||||
| chrX:77895396-77895729 | Rare:95; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chrX:78103944-78104342 | Common:4; Rare:149 | ||||
| chrX:78945179-78945422 | Rare:28 | ||||
| chrX:80335326-80335418 | Common:1; Rare:17 | ||||
| chrX:81201884-81202294 | Rare:73 | ||||
| chrX:81202323-81202657 | Common:2; Rare:46 | ||||
| chrX:85003738-85003924 | Common:2; Rare:35 | ||||
| chrX:85379601-85379810 | Common:2; Rare:28; Clinvar (benign):1 | ||||
| chrX:100593340-100593437 | Rare:13 | ||||
| chrX:100643924-100644324 | Common:1; Rare:55 |