| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:153794330-153794666 | Common:1; Rare:108; Clinvar (benign):2 | ||||
| chrX:153934977-153935334 | Common:1; Rare:81 | ||||
| chrX:154019831-154020002 | Rare:30 | ||||
| chrX:154364882-154365152 | Common:1; Rare:71; Clinvar:3; Clinvar (benign):5 | ||||
| chrX:154428466-154428704 | Common:2; Rare:41 | ||||
| chrX:154516175-154516537 | Common:4; Rare:76 | ||||
| chrX:154547546-154547660 | Common:1; Rare:27; Clinvar (benign):1 |