| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:49079775-49080001 | Rare:32 | ||||
| chrX:49123723-49123976 | Rare:54 | ||||
| chrX:49171745-49172093 | Common:4; Rare:56 | ||||
| chrX:49184887-49185066 | Common:1; Rare:23 | ||||
| chrX:49186262-49186449 | Common:1; Rare:32 | ||||
| chrX:49879399-49879599 | Rare:41 | ||||
| chrX:53082046-53082374 | Common:1; Rare:72 | ||||
| chrX:53082615-53082928 | Rare:84 | ||||
| chrX:53225157-53225504 | Common:2; Rare:114 | ||||
| chrX:53422613-53422944 | Common:2; Rare:83; Clinvar (benign):1 | ||||
| chrX:53434393-53434742 | Common:2; Rare:56 | ||||
| chrX:53536147-53536593 | Common:3; Rare:67; Clinvar:1; Clinvar (benign):1 | ||||
| chrX:53683794-53683842 | Rare:9 | ||||
| chrX:53686586-53686837 | Common:6; Rare:60 | ||||
| chrX:54358034-54358255 | Common:1; Rare:37 |