| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:14873034-14873470 | Common:1; Rare:81 | ||||
| chrX:15335499-15335671 | Common:2; Rare:41; Clinvar (benign):1 | ||||
| chrX:15790420-15790590 | Rare:35 | ||||
| chrX:16719322-16719823 | Common:1; Rare:119 | ||||
| chrX:16786201-16786548 | Common:2; Rare:76 | ||||
| chrX:19343715-19344002 | Common:5; Rare:77 | ||||
| chrX:19670880-19670972 | Rare:17 | ||||
| chrX:19670987-19671039 | Rare:7 | ||||
| chrX:20267043-20267281 | Common:1; Rare:44 | ||||
| chrX:21940464-21940834 | Common:2; Rare:95 | ||||
| chrX:23743175-23743442 | Common:6; Rare:55 | ||||
| chrX:23782984-23783289 | Common:5; Rare:66 | ||||
| chrX:23783352-23783923 | Common:4; Rare:145 | ||||
| chrX:23907700-23908169 | Common:1; Rare:105 | ||||
| chrX:24054597-24055037 | Common:2; Rare:103 |