| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:71254681-71254764 | Common:1; Rare:8 | ||||
| chrX:72079650-72080012 | Rare:59 | ||||
| chrX:73563055-73563318 | Common:1; Rare:35 | ||||
| chrX:74421384-74421572 | Common:1; Rare:55; Clinvar (benign):3 | ||||
| chrX:74614422-74614833 | Common:1; Rare:90 | ||||
| chrX:75156268-75156369 | Common:2; Rare:26 | ||||
| chrX:75274636-75274727 | Common:1; Rare:15 | ||||
| chrX:75523013-75523212 | Common:1; Rare:41 | ||||
| chrX:75523231-75523302 | Rare:10 | ||||
| chrX:77895355-77895750 | Rare:116; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chrX:78103951-78104376 | Common:4; Rare:155 | ||||
| chrX:78139576-78139713 | Common:1; Rare:72 | ||||
| chrX:80809870-80810151 | Rare:36 | ||||
| chrX:81201876-81202675 | Common:2; Rare:124 | ||||
| chrX:96685048-96685098 | Rare:8 |