| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:101390725-101391044 | Rare:78 | ||||
| chrX:101407893-101408307 | Common:5; Rare:77; Clinvar:1; Clinvar (benign):10 | ||||
| chrX:101418000-101418304 | Common:2; Rare:49 | ||||
| chrX:101485331-101485503 | Rare:21 | ||||
| chrX:101550430-101550610 | Rare:29 | ||||
| chrX:102125529-102125795 | Common:2; Rare:46 | ||||
| chrX:102142389-102142583 | Rare:48 | ||||
| chrX:102651303-102651559 | Common:2; Rare:66 | ||||
| chrX:103330116-103330275 | Rare:23 | ||||
| chrX:103356122-103356180 | Rare:8 | ||||
| chrX:103356277-103356916 | Common:4; Rare:96 | ||||
| chrX:103585349-103585447 | Rare:10 | ||||
| chrX:103585455-103585682 | Common:3; Rare:46 | ||||
| chrX:103607806-103608070 | Rare:48 | ||||
| chrX:103628669-103629023 | Common:1; Rare:45 |