| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:1392056-1392474 | Common:7; Rare:182 | ||||
| chrX:2828684-2828982 | Common:3; Rare:47 | ||||
| chrX:6226287-6226417 | Common:1; Rare:16 | ||||
| chrX:6228838-6229038 | Common:1; Rare:38 | ||||
| chrX:7927371-7927479 | Common:1; Rare:30 | ||||
| chrX:7927695-7927993 | Common:2; Rare:65 | ||||
| chrX:10620383-10620689 | Common:3; Rare:46 | ||||
| chrX:11111136-11111362 | Common:3; Rare:49 | ||||
| chrX:12974918-12975161 | Common:1; Rare:63 | ||||
| chrX:13734529-13734866 | Common:3; Rare:101; Clinvar (benign):1 | ||||
| chrX:14029796-14029980 | Common:1; Rare:60 | ||||
| chrX:14873035-14873461 | Common:1; Rare:80 | ||||
| chrX:15335502-15335763 | Common:3; Rare:57; Clinvar (benign):1 | ||||
| chrX:15790397-15790575 | Rare:40 | ||||
| chrX:16123365-16123586 | Rare:34 |