| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:49075641-49075937 | Rare:48; Clinvar:1; Clinvar (benign):4 | ||||
| chrX:49079818-49079949 | Rare:18 | ||||
| chrX:49171745-49172035 | Common:4; Rare:38 | ||||
| chrX:49879397-49879551 | Rare:28 | ||||
| chrX:51893308-51893691 | Common:2; Rare:76 | ||||
| chrX:53422616-53422918 | Common:2; Rare:82; Clinvar (benign):1 | ||||
| chrX:54043926-54044029 | Rare:21 | ||||
| chrX:54044453-54044590 | Rare:35 | ||||
| chrX:54440250-54440459 | Rare:41 | ||||
| chrX:54530047-54530312 | Common:2; Rare:38 | ||||
| chrX:55000204-55000420 | Common:1; Rare:51 | ||||
| chrX:55161090-55161292 | Rare:62 | ||||
| chrX:56232286-56232458 | Rare:25 | ||||
| chrX:56563453-56563658 | Rare:44; Clinvar:1 | ||||
| chrX:57121422-57121598 | Common:1; Rare:41 |