| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:154478749-154479130 | Common:5; Rare:147 | ||||
| chrX:154479187-154479341 | Rare:48 | ||||
| chrX:154486568-154486772 | Rare:59 | ||||
| chrX:154490589-154490815 | Common:4; Rare:97 | ||||
| chrX:154516175-154516537 | Common:8; Rare:144 | ||||
| chrX:154540915-154541328 | Rare:107 | ||||
| chrX:154541898-154542300 | Rare:135; Clinvar:2 | ||||
| chrX:154546795-154547006 | Rare:146 | ||||
| chrX:154547080-154547450 | Rare:111 | ||||
| chrX:154547522-154547645 | Common:1; Rare:30; Clinvar (benign):1 | ||||
| chrX:154547550-154547681 | Common:1; Rare:35; Clinvar (benign):1 | ||||
| chrX:154762374-154763094 | Common:9; Rare:248; Clinvar:5 | ||||
| chrX:154805353-154805562 | Rare:77 | ||||
| chrX:155026687-155026924 | Common:2; Rare:101 | ||||
| chrX:155071056-155071551 | Common:2; Rare:202 |