| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:23783518-23783709 | Common:2; Rare:41 | ||||
| chrX:23785305-23785564 | Common:1; Rare:48 | ||||
| chrX:23907707-23908097 | Common:1; Rare:86 | ||||
| chrX:24054902-24055006 | Rare:39 | ||||
| chrX:24149594-24149774 | Rare:30 | ||||
| chrX:24465218-24465380 | Common:3; Rare:46 | ||||
| chrX:24693809-24693956 | Common:1; Rare:27 | ||||
| chrX:30653171-30653504 | Common:2; Rare:86 | ||||
| chrX:31266905-31267035 | Common:1; Rare:43 | ||||
| chrX:33128214-33128506 | Common:1; Rare:39 | ||||
| chrX:37847506-37847677 | Common:1; Rare:43 | ||||
| chrX:41085734-41085877 | Rare:35 | ||||
| chrX:41334421-41334697 | Common:2; Rare:109 | ||||
| chrX:41334993-41335129 | Common:1; Rare:17 | ||||
| chrX:43973387-43973581 | Common:1; Rare:29; Clinvar (benign):1 |