| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:28587020-28587140 | Rare:11 | ||||
| chrX:30308973-30309445 | Common:3; Rare:266; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chrX:30652443-30653102 | Common:3; Rare:102 | ||||
| chrX:30653134-30653423 | Common:2; Rare:77 | ||||
| chrX:30889252-30889613 | Common:1; Rare:60 | ||||
| chrX:31266916-31267035 | Common:1; Rare:39 | ||||
| chrX:31435545-31435945 | Common:3; Rare:95 | ||||
| chrX:31508506-31508910 | Common:5; Rare:92 | ||||
| chrX:34657246-34657699 | Common:2; Rare:118 | ||||
| chrX:37349170-37349398 | Common:2; Rare:33 | ||||
| chrX:37847597-37847779 | Common:1; Rare:30 | ||||
| chrX:38327207-38327319 | Common:1; Rare:20 | ||||
| chrX:38327504-38327736 | Rare:60 | ||||
| chrX:38561369-38561561 | Common:3; Rare:49; Clinvar (benign):1 | ||||
| chrX:38801162-38801495 | Common:1; Rare:65 |