| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:154097684-154098110 | Common:1; Rare:73; Clinvar:2; Clinvar (benign):2 | ||||
| chrX:154135976-154137138 | Common:14; Rare:279 | ||||
| chrX:154371214-154371521 | Common:1; Rare:66; Clinvar:3; Clinvar (benign):5 | ||||
| chrX:154378382-154379328 | Common:1; Rare:342 | ||||
| chrX:154397486-154397886 | Common:2; Rare:126 | ||||
| chrX:154398058-154398381 | Common:3; Rare:81 | ||||
| chrX:154411320-154411690 | Rare:72 | ||||
| chrX:154412086-154412272 | Common:1; Rare:20; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chrX:154428436-154428693 | Common:2; Rare:46 | ||||
| chrX:154436700-154436930 | Common:2; Rare:31 | ||||
| chrX:154436967-154437201 | Rare:61 | ||||
| chrX:154478770-154479150 | Common:4; Rare:110 | ||||
| chrX:154479170-154479450 | Rare:50 | ||||
| chrX:154486582-154486870 | Common:1; Rare:55 | ||||
| chrX:154490593-154490973 | Common:2; Rare:72 |