| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:65034729-65034823 | Common:1; Rare:19 | ||||
| chrX:67543887-67544101 | Rare:39 | ||||
| chrX:67544355-67544514 | Rare:16 | ||||
| chrX:68433320-68433560 | Rare:32 | ||||
| chrX:68498965-68499059 | Rare:22 | ||||
| chrX:68828837-68829030 | Rare:38 | ||||
| chrX:70289875-70290099 | Rare:42 | ||||
| chrX:71365937-71366256 | Common:3; Rare:58 | ||||
| chrX:71532856-71533154 | Rare:56 | ||||
| chrX:72181556-72181779 | Common:2; Rare:58 | ||||
| chrX:73563423-73563494 | Rare:32 | ||||
| chrX:74421377-74421553 | Common:1; Rare:52; Clinvar (benign):3 | ||||
| chrX:75156020-75156319 | Common:2; Rare:81; Clinvar (benign):2 | ||||
| chrX:75274608-75274708 | Common:2; Rare:21 | ||||
| chrX:75523018-75523137 | Rare:27 |