| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:12975458-12975755 | Common:2; Rare:62 | ||||
| chrX:12975801-12976361 | Common:4; Rare:104 | ||||
| chrX:13734540-13735083 | Common:3; Rare:149; Clinvar (benign):1 | ||||
| chrX:14029800-14030009 | Common:2; Rare:62 | ||||
| chrX:14873040-14873463 | Common:1; Rare:79 | ||||
| chrX:15500577-15500870 | Common:1; Rare:44 | ||||
| chrX:15507017-15507331 | Rare:34 | ||||
| chrX:15854701-15855036 | Rare:70 | ||||
| chrX:16712579-16712704 | Common:1; Rare:20 | ||||
| chrX:16719349-16719802 | Common:1; Rare:105 | ||||
| chrX:16786150-16786539 | Common:3; Rare:83 | ||||
| chrX:16870313-16870729 | Common:2; Rare:102 | ||||
| chrX:17861296-17861529 | Common:1; Rare:26 | ||||
| chrX:18984049-18984244 | Common:1; Rare:44 | ||||
| chrX:19343716-19344040 | Common:5; Rare:87; Clinvar (benign):1 |