| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:2691175-2691526 | Common:9; Rare:165 | ||||
| chrX:7927377-7927460 | Common:1; Rare:25 | ||||
| chrX:7927695-7927769 | Rare:12 | ||||
| chrX:10576844-10577084 | Common:1; Rare:46 | ||||
| chrX:11111184-11111478 | Common:4; Rare:51 | ||||
| chrX:11665112-11665366 | Rare:42 | ||||
| chrX:11759469-11759673 | Rare:25 | ||||
| chrX:12791231-12791503 | Rare:55 | ||||
| chrX:12975005-12975232 | Common:2; Rare:53 | ||||
| chrX:13652996-13653173 | Rare:37 | ||||
| chrX:13688969-13689269 | Common:2; Rare:80 | ||||
| chrX:13734526-13734870 | Common:3; Rare:101; Clinvar (benign):1 | ||||
| chrX:14029801-14030104 | Common:3; Rare:79 | ||||
| chrX:14873040-14873470 | Common:1; Rare:80 | ||||
| chrX:15854701-15854915 | Rare:45 |