| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:56995488-56995688 | Common:1; Rare:45 | ||||
| chrX:57121472-57121678 | Common:1; Rare:49 | ||||
| chrX:63755068-63755386 | Rare:66 | ||||
| chrX:63785159-63785267 | Rare:29 | ||||
| chrX:64205690-64205887 | Rare:30 | ||||
| chrX:65034694-65034827 | Common:1; Rare:27 | ||||
| chrX:68433466-68433614 | Rare:30 | ||||
| chrX:68498961-68499059 | Rare:22 | ||||
| chrX:68828837-68829021 | Rare:37 | ||||
| chrX:70133198-70133483 | Common:2; Rare:44 | ||||
| chrX:70289881-70290130 | Rare:46 | ||||
| chrX:70931093-70931203 | Common:2; Rare:9 | ||||
| chrX:71118462-71118748 | Common:1; Rare:57; Clinvar (benign):2 | ||||
| chrX:71254691-71254846 | Common:1; Rare:14 | ||||
| chrX:71532883-71533121 | Rare:45 |