| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:153934974-153935339 | Common:1; Rare:84 | ||||
| chrX:153971184-153971296 | Rare:26 | ||||
| chrX:154019782-154020003 | Rare:42 | ||||
| chrX:154354630-154355070 | Common:1; Rare:119; Clinvar:12; Clinvar (benign):14; Clinvar (pathogenic):1 | ||||
| chrX:154409192-154409464 | Rare:41 | ||||
| chrX:154428472-154428749 | Common:3; Rare:56; Clinvar:1 | ||||
| chrX:154486562-154486760 | Rare:29 | ||||
| chrX:154547541-154547669 | Common:1; Rare:32; Clinvar (benign):1 | ||||
| chrX:155026800-155027063 | Rare:74 |