| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:16870195-16870738 | Common:3; Rare:126 | ||||
| chrX:18354672-18354745 | Common:1; Rare:13 | ||||
| chrX:18425356-18425638 | Common:2; Rare:70; Clinvar:1; Clinvar (benign):3 | ||||
| chrX:18984055-18984211 | Rare:36 | ||||
| chrX:19343673-19344049 | Common:6; Rare:105; Clinvar (benign):1 | ||||
| chrX:19670329-19670698 | Common:2; Rare:50 | ||||
| chrX:19670868-19671148 | Common:1; Rare:46 | ||||
| chrX:19671150-19671240 | Rare:7 | ||||
| chrX:20141724-20142117 | Common:1; Rare:87 | ||||
| chrX:20267057-20267141 | Rare:15 | ||||
| chrX:21374095-21374506 | Common:5; Rare:92 | ||||
| chrX:21839490-21839684 | Rare:44 | ||||
| chrX:21940607-21940871 | Common:2; Rare:66 | ||||
| chrX:23333353-23333709 | Rare:61 | ||||
| chrX:23334107-23334436 | Common:2; Rare:73 |