| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:276248-276375 | Common:3; Rare:43 | ||||
| chrX:386945-386993 | Rare:12 | ||||
| chrX:1391897-1392371 | Common:6; Rare:203 | ||||
| chrX:2691168-2691526 | Common:9; Rare:167 | ||||
| chrX:2929273-2929513 | Common:2; Rare:68 | ||||
| chrX:7927377-7927449 | Common:1; Rare:24 | ||||
| chrX:7927697-7927764 | Rare:10 | ||||
| chrX:11111259-11111356 | Common:2; Rare:23 | ||||
| chrX:11665088-11665371 | Rare:48 | ||||
| chrX:11758049-11758339 | Common:2; Rare:43 | ||||
| chrX:11759476-11759669 | Rare:24 | ||||
| chrX:13652964-13653196 | Rare:51 | ||||
| chrX:13734529-13734854 | Common:3; Rare:99; Clinvar (benign):1 | ||||
| chrX:14029801-14030104 | Common:3; Rare:79 | ||||
| chrX:14873045-14873495 | Common:1; Rare:84 |