| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:71365859-71366371 | Common:4; Rare:112; Clinvar (benign):1 | ||||
| chrX:71366494-71366586 | Common:3; Rare:32 | ||||
| chrX:71532894-71533155 | Rare:51 | ||||
| chrX:72181344-72181660 | Common:3; Rare:75 | ||||
| chrX:72238928-72239166 | Common:4; Rare:74 | ||||
| chrX:72305890-72305994 | Rare:26 | ||||
| chrX:72306585-72306850 | Common:1; Rare:42 | ||||
| chrX:72307039-72307101 | Rare:8 | ||||
| chrX:72307140-72307240 | Rare:15 | ||||
| chrX:73563024-73563318 | Common:1; Rare:43 | ||||
| chrX:74614221-74614331 | Rare:19 | ||||
| chrX:74614458-74614823 | Common:1; Rare:81 | ||||
| chrX:75156018-75156378 | Common:3; Rare:98; Clinvar (benign):2 | ||||
| chrX:75274020-75274175 | Rare:23 | ||||
| chrX:75274636-75274708 | Common:1; Rare:13 |