| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:14873049-14873470 | Common:1; Rare:80 | ||||
| chrX:15270137-15270267 | Rare:16 | ||||
| chrX:15335511-15335781 | Common:3; Rare:57; Clinvar (benign):1 | ||||
| chrX:15854701-15854902 | Rare:40 | ||||
| chrX:16719424-16719791 | Rare:92 | ||||
| chrX:16786163-16786490 | Common:2; Rare:66 | ||||
| chrX:18984105-18984238 | Common:1; Rare:25 | ||||
| chrX:21374110-21374485 | Common:3; Rare:87 | ||||
| chrX:21940613-21940794 | Common:2; Rare:50 | ||||
| chrX:23334116-23334411 | Common:2; Rare:63 | ||||
| chrX:23783036-23783423 | Common:4; Rare:81 | ||||
| chrX:23785297-23785577 | Common:1; Rare:51 | ||||
| chrX:23907712-23908049 | Common:1; Rare:72 | ||||
| chrX:24054890-24055030 | Rare:50 | ||||
| chrX:24149594-24149789 | Rare:33 |