| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:12975005-12975265 | Common:2; Rare:59 | ||||
| chrX:13734543-13734815 | Common:3; Rare:86; Clinvar (benign):1 | ||||
| chrX:14029801-14030046 | Common:3; Rare:74 | ||||
| chrX:14873214-14873470 | Rare:45 | ||||
| chrX:15790397-15790543 | Rare:35 | ||||
| chrX:16719444-16719690 | Rare:71 | ||||
| chrX:16786201-16786496 | Common:1; Rare:59 | ||||
| chrX:19343738-19343997 | Common:4; Rare:73 | ||||
| chrX:19670876-19671054 | Rare:33 | ||||
| chrX:20141757-20142071 | Common:1; Rare:69 | ||||
| chrX:20267045-20267285 | Common:1; Rare:45 | ||||
| chrX:21839459-21839679 | Common:1; Rare:51 | ||||
| chrX:21940412-21940864 | Common:3; Rare:105 | ||||
| chrX:23743215-23743493 | Common:7; Rare:53 | ||||
| chrX:23782961-23783263 | Common:5; Rare:67 |