| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:100644062-100644313 | Common:1; Rare:31 | ||||
| chrX:101051844-101052203 | Common:2; Rare:64 | ||||
| chrX:101407891-101408289 | Common:5; Rare:73; Clinvar:1; Clinvar (benign):10 | ||||
| chrX:101418214-101418396 | Common:2; Rare:31 | ||||
| chrX:101622908-101623215 | Common:2; Rare:49 | ||||
| chrX:102142421-102142580 | Rare:39 | ||||
| chrX:102651303-102651562 | Common:2; Rare:67 | ||||
| chrX:103356444-103356610 | Common:3; Rare:17 | ||||
| chrX:103376403-103376613 | Common:1; Rare:34 | ||||
| chrX:103502841-103503096 | Common:2; Rare:30 | ||||
| chrX:103585454-103585682 | Common:3; Rare:46 | ||||
| chrX:103607814-103608067 | Rare:48 | ||||
| chrX:103628669-103629023 | Common:1; Rare:45 | ||||
| chrX:103686685-103687046 | Common:4; Rare:48 | ||||
| chrX:103688008-103688439 | Common:1; Rare:51 |