| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:100820208-100820432 | Common:2; Rare:52 | ||||
| chrX:100928621-100928631 | Rare:1 | ||||
| chrX:100928829-100929023 | Common:1; Rare:31 | ||||
| chrX:101407893-101408313 | Common:5; Rare:79; Clinvar:1; Clinvar (benign):10 | ||||
| chrX:103585481-103585652 | Common:3; Rare:39 | ||||
| chrX:103586475-103586736 | Rare:52 | ||||
| chrX:103607665-103607988 | Common:1; Rare:51 | ||||
| chrX:103629448-103629522 | Rare:19 | ||||
| chrX:103686685-103686895 | Common:1; Rare:33 | ||||
| chrX:103687068-103687304 | Rare:41 | ||||
| chrX:103688006-103688296 | Common:1; Rare:34 | ||||
| chrX:104156894-104157080 | Common:1; Rare:30 | ||||
| chrX:107628425-107628520 | Common:1; Rare:11; Clinvar (benign):1 | ||||
| chrX:107716147-107716390 | Rare:42 | ||||
| chrX:107716462-107716785 | Common:1; Rare:53 |