| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:153971178-153971298 | Rare:29 | ||||
| chrX:153971796-153971967 | Rare:48 | ||||
| chrX:154371193-154371490 | Common:1; Rare:67; Clinvar:4; Clinvar (benign):6 | ||||
| chrX:154409255-154409523 | Rare:53 | ||||
| chrX:154428462-154428689 | Common:2; Rare:39 | ||||
| chrX:154547543-154547639 | Common:1; Rare:25; Clinvar (benign):1 | ||||
| chrX:154762569-154762938 | Common:4; Rare:83; Clinvar:2 | ||||
| chrX:155026680-155026987 | Common:1; Rare:74 | ||||
| chrX:155027007-155027068 | Rare:19 | ||||
| chrX:155071084-155071520 | Common:1; Rare:95 | ||||
| chrX:155216261-155216501 | Rare:44 | ||||
| chrX:155612893-155612979 | Rare:16 |