| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:48901991-48902225 | Rare:43; Clinvar:2; Clinvar (benign):2 | ||||
| chrX:49156245-49156443 | Common:2; Rare:47 | ||||
| chrX:51395718-51395961 | Rare:38 | ||||
| chrX:53093872-53094224 | Rare:64 | ||||
| chrX:53145664-53145894 | Common:4; Rare:39 | ||||
| chrX:53193328-53193470 | Rare:25; Clinvar:1; Clinvar (benign):1 | ||||
| chrX:53201711-53201926 | Common:1; Rare:36; Clinvar (benign):1 | ||||
| chrX:53558977-53559257 | Rare:44 | ||||
| chrX:54443135-54443491 | Common:2; Rare:45 | ||||
| chrX:54769386-54769614 | Common:1; Rare:30 | ||||
| chrX:55489832-55489996 | Rare:19 | ||||
| chrX:55908044-55908502 | Rare:75 | ||||
| chrX:56564365-56564444 | Common:1; Rare:10 | ||||
| chrX:66015282-66015463 | Common:2; Rare:27 | ||||
| chrX:68996054-68996193 | Rare:17 |