| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:20116870-20117070 | Common:1; Rare:44 | ||||
| chrX:20141761-20142083 | Common:1; Rare:72 | ||||
| chrX:21374142-21374486 | Common:1; Rare:71 | ||||
| chrX:21940489-21940848 | Common:2; Rare:91 | ||||
| chrX:23782958-23783330 | Common:5; Rare:78 | ||||
| chrX:23907706-23908049 | Common:1; Rare:73 | ||||
| chrX:24054870-24055009 | Rare:51 | ||||
| chrX:24149563-24149743 | Rare:27 | ||||
| chrX:38327472-38327612 | Rare:33 | ||||
| chrX:38561264-38561564 | Common:3; Rare:80; Clinvar (benign):1 | ||||
| chrX:43973387-43973581 | Common:1; Rare:29; Clinvar (benign):1 | ||||
| chrX:44542796-44543034 | Common:1; Rare:48 | ||||
| chrX:46447188-46447338 | Rare:27 | ||||
| chrX:46545377-46545540 | Common:1; Rare:33; Clinvar (benign):1 | ||||
| chrX:47144609-47144866 | Common:1; Rare:47 |