| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:11111141-11111359 | Common:3; Rare:46 | ||||
| chrX:12974964-12975168 | Common:2; Rare:53 | ||||
| chrX:12976148-12976361 | Rare:45 | ||||
| chrX:13652972-13653203 | Rare:53 | ||||
| chrX:13734569-13734889 | Common:3; Rare:93; Clinvar (benign):1 | ||||
| chrX:14873041-14873103 | Rare:8 | ||||
| chrX:14873342-14873463 | Rare:22 | ||||
| chrX:15790397-15790563 | Rare:39 | ||||
| chrX:16786201-16786483 | Common:1; Rare:54 | ||||
| chrX:19343701-19343997 | Common:6; Rare:83 | ||||
| chrX:21374153-21374439 | Rare:60 | ||||
| chrX:21940607-21940759 | Common:2; Rare:41 | ||||
| chrX:23667356-23667613 | Common:2; Rare:82 | ||||
| chrX:23782903-23783230 | Common:6; Rare:66 | ||||
| chrX:23907838-23908068 | Rare:43 |