| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:45807065-45807138 | Rare:14 | ||||
| chrX:46469551-46469880 | Common:1; Rare:31 | ||||
| chrX:47129494-47129630 | Common:2; Rare:16 | ||||
| chrX:47206049-47206437 | Common:4; Rare:64; Clinvar:1; Clinvar (benign):5 | ||||
| chrX:47212766-47213044 | Rare:57; Clinvar:1; Clinvar (benign):1 | ||||
| chrX:47214392-47214637 | Rare:45; Clinvar (benign):3 | ||||
| chrX:47566643-47567084 | Common:1; Rare:111 | ||||
| chrX:48928564-48928763 | Common:1; Rare:19 | ||||
| chrX:49173134-49173482 | Rare:80 | ||||
| chrX:49881642-49881956 | Common:3; Rare:32 | ||||
| chrX:53054763-53055062 | Rare:29 | ||||
| chrX:53055904-53056130 | Common:2; Rare:27 | ||||
| chrX:54931375-54931524 | Rare:15 | ||||
| chrX:55453070-55453142 | Rare:14 | ||||
| chrX:55489847-55489878 | Rare:2 |