| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:70289865-70290075 | Rare:41 | ||||
| chrX:71068299-71068462 | Common:1; Rare:49 | ||||
| chrX:71118659-71118748 | Rare:28; Clinvar (benign):2 | ||||
| chrX:71532889-71533152 | Rare:51 | ||||
| chrX:75156247-75156382 | Common:2; Rare:41 | ||||
| chrX:75273986-75274223 | Rare:32 | ||||
| chrX:75274610-75274692 | Common:2; Rare:17 | ||||
| chrX:75522996-75523163 | Rare:39 | ||||
| chrX:75523167-75523270 | Common:1; Rare:17 | ||||
| chrX:75523274-75523562 | Common:3; Rare:39 | ||||
| chrX:77786186-77786324 | Common:1; Rare:17 | ||||
| chrX:77895412-77895750 | Rare:93; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chrX:78103944-78104332 | Common:4; Rare:146 | ||||
| chrX:78139586-78139745 | Common:2; Rare:73 | ||||
| chrX:80335326-80335407 | Common:1; Rare:13 |