| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:7927703-7927799 | Rare:23 | ||||
| chrX:11111199-11111365 | Common:3; Rare:34 | ||||
| chrX:11759476-11759669 | Rare:24 | ||||
| chrX:12791302-12791611 | Common:1; Rare:60 | ||||
| chrX:12975079-12975196 | Common:1; Rare:33 | ||||
| chrX:13734526-13734866 | Common:3; Rare:101; Clinvar (benign):1 | ||||
| chrX:13735057-13735163 | Common:1; Rare:27; Clinvar (benign):1 | ||||
| chrX:14029783-14030046 | Common:3; Rare:76 | ||||
| chrX:14873035-14873533 | Common:2; Rare:96 | ||||
| chrX:15493230-15493415 | Common:1; Rare:32 | ||||
| chrX:16719316-16719791 | Rare:111 | ||||
| chrX:18425346-18425615 | Common:2; Rare:63; Clinvar:1; Clinvar (benign):3 | ||||
| chrX:18984112-18984220 | Rare:22 | ||||
| chrX:23783235-23783319 | Rare:18 | ||||
| chrX:23907709-23907797 | Common:1; Rare:20 |