| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:103310590-103310715 | Common:1; Rare:19 | ||||
| chrX:103310889-103311143 | Common:2; Rare:33 | ||||
| chrX:103330116-103330291 | Rare:25 | ||||
| chrX:103356177-103356603 | Common:4; Rare:57 | ||||
| chrX:103376193-103376311 | Common:1; Rare:20 | ||||
| chrX:103376324-103376607 | Common:1; Rare:42 | ||||
| chrX:103585445-103585682 | Common:3; Rare:47 | ||||
| chrX:103586465-103586783 | Rare:67 | ||||
| chrX:103607849-103608025 | Rare:34 | ||||
| chrX:103628777-103629003 | Common:1; Rare:30 | ||||
| chrX:103629443-103629535 | Rare:26 | ||||
| chrX:103686653-103686895 | Common:1; Rare:41 | ||||
| chrX:103687997-103688183 | Common:1; Rare:30 | ||||
| chrX:103776716-103776997 | Common:2; Rare:39; Clinvar (benign):1 | ||||
| chrX:103919000-103919194 | Common:4; Rare:34 |