| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:44542796-44543034 | Common:1; Rare:48 | ||||
| chrX:46545377-46545556 | Common:1; Rare:39; Clinvar (benign):1 | ||||
| chrX:47144609-47144837 | Common:1; Rare:41 | ||||
| chrX:47145047-47145301 | Rare:36 | ||||
| chrX:47232912-47233040 | Rare:38 | ||||
| chrX:47233235-47233444 | Rare:35 | ||||
| chrX:47482556-47482665 | Common:5; Rare:24; Clinvar:2 | ||||
| chrX:47659071-47659237 | Rare:51 | ||||
| chrX:47836651-47836968 | Common:1; Rare:64 | ||||
| chrX:48476144-48476230 | Rare:20 | ||||
| chrX:48801674-48801991 | Rare:59 | ||||
| chrX:48911643-48911719 | Rare:15; Clinvar (benign):2 | ||||
| chrX:48919007-48919288 | Rare:45 | ||||
| chrX:48958363-48958671 | Rare:55 | ||||
| chrX:49073991-49074183 | Rare:47 |