| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:100731437-100731570 | Rare:20 | ||||
| chrX:100820273-100820449 | Common:2; Rare:40 | ||||
| chrX:101348660-101349044 | Common:4; Rare:75; Clinvar:1; Clinvar (benign):2 | ||||
| chrX:101386150-101386379 | Rare:29 | ||||
| chrX:101390747-101391059 | Rare:79 | ||||
| chrX:101407799-101408282 | Common:5; Rare:86; Clinvar:2; Clinvar (benign):11 | ||||
| chrX:101623051-101623241 | Rare:36 | ||||
| chrX:102651318-102651569 | Common:2; Rare:67 | ||||
| chrX:103376406-103376607 | Common:1; Rare:33 | ||||
| chrX:103585455-103585682 | Common:3; Rare:46 | ||||
| chrX:103586444-103586700 | Rare:53 | ||||
| chrX:103607875-103608025 | Rare:27 | ||||
| chrX:103629351-103629522 | Common:1; Rare:48 | ||||
| chrX:103686653-103687345 | Common:5; Rare:110 | ||||
| chrX:103688008-103688233 | Common:1; Rare:30 |