| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:386696-387012 | Common:2; Rare:132 | ||||
| chrX:1392035-1392367 | Common:6; Rare:147 | ||||
| chrX:2929257-2929513 | Common:2; Rare:70 | ||||
| chrX:2964541-2964666 | Common:2; Rare:22 | ||||
| chrX:3347010-3347184 | Common:2; Rare:31 | ||||
| chrX:7927371-7927498 | Common:1; Rare:34 | ||||
| chrX:7927697-7927786 | Rare:22 | ||||
| chrX:10589938-10590290 | Common:8; Rare:95 | ||||
| chrX:10620412-10620693 | Common:1; Rare:43 | ||||
| chrX:11111136-11111382 | Common:4; Rare:53 | ||||
| chrX:11759476-11759657 | Rare:21 | ||||
| chrX:12975005-12975307 | Common:2; Rare:69 | ||||
| chrX:13689090-13689188 | Rare:31 | ||||
| chrX:13734557-13734854 | Common:3; Rare:90; Clinvar (benign):1 | ||||
| chrX:14029801-14030111 | Common:3; Rare:81 |