| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:13653005-13653221 | Rare:50 | ||||
| chrX:13688969-13689280 | Common:2; Rare:83 | ||||
| chrX:13734540-13734859 | Common:3; Rare:96; Clinvar (benign):1 | ||||
| chrX:14873049-14873495 | Common:1; Rare:84 | ||||
| chrX:15493205-15493424 | Common:1; Rare:36 | ||||
| chrX:15738140-15738339 | Rare:35 | ||||
| chrX:16719411-16719727 | Rare:86 | ||||
| chrX:16786175-16786567 | Common:2; Rare:86 | ||||
| chrX:16870039-16870744 | Common:3; Rare:161 | ||||
| chrX:18354672-18354745 | Common:1; Rare:13 | ||||
| chrX:18984048-18984244 | Common:1; Rare:44 | ||||
| chrX:19355644-19355737 | Common:2; Rare:18; Clinvar (benign):4 | ||||
| chrX:20267020-20267139 | Rare:23 | ||||
| chrX:21374109-21374600 | Common:4; Rare:110 | ||||
| chrX:21839457-21839686 | Common:1; Rare:55 |