| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:276238-276375 | Common:3; Rare:47 | ||||
| chrX:1391900-1392020 | Rare:45 | ||||
| chrX:1392022-1392349 | Common:6; Rare:152 | ||||
| chrX:2929269-2929513 | Common:2; Rare:68 | ||||
| chrX:7927379-7927512 | Common:1; Rare:33 | ||||
| chrX:7927710-7927801 | Rare:21 | ||||
| chrX:11111136-11111382 | Common:4; Rare:53 | ||||
| chrX:11758059-11758266 | Common:2; Rare:36 | ||||
| chrX:12975076-12975166 | Rare:29 | ||||
| chrX:13734529-13734866 | Common:3; Rare:101; Clinvar (benign):1 | ||||
| chrX:14873040-14873463 | Common:1; Rare:79 | ||||
| chrX:15500597-15500866 | Common:1; Rare:40 | ||||
| chrX:15854721-15854959 | Rare:55 | ||||
| chrX:16719289-16719690 | Rare:97 | ||||
| chrX:19343716-19344004 | Common:5; Rare:77 |