| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:48574235-48574565 | Common:2; Rare:98 | ||||
| chrX:48574880-48575241 | Common:3; Rare:87 | ||||
| chrX:48576381-48576573 | Common:1; Rare:60 | ||||
| chrX:48683687-48683893 | Rare:38 | ||||
| chrX:48919012-48919277 | Rare:43 | ||||
| chrX:48958367-48958679 | Rare:55 | ||||
| chrX:49002220-49002543 | Common:2; Rare:56 | ||||
| chrX:49079835-49079948 | Rare:16 | ||||
| chrX:49123728-49123963 | Rare:51 | ||||
| chrX:49171780-49172013 | Common:3; Rare:29 | ||||
| chrX:53082038-53082386 | Common:1; Rare:75 | ||||
| chrX:53082933-53083567 | Rare:139 | ||||
| chrX:53225195-53225491 | Common:2; Rare:94 | ||||
| chrX:53422601-53422984 | Common:2; Rare:95; Clinvar (benign):1 | ||||
| chrX:53684092-53684468 | Rare:98 |