| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:43973387-43973459 | Rare:7 | ||||
| chrX:46545389-46545571 | Rare:45 | ||||
| chrX:47144682-47144813 | Rare:21 | ||||
| chrX:47483166-47483237 | Common:1; Rare:10 | ||||
| chrX:48508848-48509036 | Common:1; Rare:38 | ||||
| chrX:48527015-48527276 | Rare:46; Clinvar (benign):2 | ||||
| chrX:48574172-48574558 | Common:3; Rare:102 | ||||
| chrX:49171776-49171983 | Common:3; Rare:25 | ||||
| chrX:53422645-53422902 | Common:1; Rare:62 | ||||
| chrX:55000207-55000420 | Common:1; Rare:51 | ||||
| chrX:57121460-57121626 | Common:1; Rare:40 | ||||
| chrX:65034711-65034826 | Common:1; Rare:25 | ||||
| chrX:68498968-68499058 | Rare:22 | ||||
| chrX:70289872-70290137 | Rare:50 | ||||
| chrX:71118504-71118748 | Common:1; Rare:49; Clinvar (benign):2 |