| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:24465039-24465369 | Common:4; Rare:94 | ||||
| chrX:24693812-24693949 | Common:1; Rare:26 | ||||
| chrX:30653104-30653540 | Common:2; Rare:113 | ||||
| chrX:34657286-34657484 | Rare:54 | ||||
| chrX:37572052-37572375 | Common:1; Rare:107 | ||||
| chrX:37847489-37847637 | Rare:37 | ||||
| chrX:38006486-38006630 | Rare:14 | ||||
| chrX:38801247-38801516 | Common:2; Rare:50 | ||||
| chrX:40735204-40735640 | Rare:104 | ||||
| chrX:41085124-41085922 | Common:4; Rare:207 | ||||
| chrX:41334999-41335374 | Common:2; Rare:67 | ||||
| chrX:41689003-41689070 | Common:1; Rare:6 | ||||
| chrX:43656117-43656441 | Rare:60 | ||||
| chrX:46545371-46545556 | Common:1; Rare:40; Clinvar (benign):1 | ||||
| chrX:46836677-46837090 | Rare:77; Clinvar:3; Clinvar (benign):1 |