| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:101390806-101391046 | Rare:70 | ||||
| chrX:101407893-101408292 | Common:5; Rare:73; Clinvar:1; Clinvar (benign):10 | ||||
| chrX:101418223-101418384 | Common:2; Rare:24 | ||||
| chrX:101623016-101623215 | Rare:37 | ||||
| chrX:102651325-102651559 | Common:2; Rare:61 | ||||
| chrX:103255092-103255243 | Rare:16 | ||||
| chrX:103356285-103356603 | Common:4; Rare:44 | ||||
| chrX:103376401-103376613 | Common:1; Rare:34 | ||||
| chrX:103376827-103377106 | Common:2; Rare:40 | ||||
| chrX:103585455-103585675 | Common:3; Rare:45 | ||||
| chrX:103607642-103608042 | Common:1; Rare:61 | ||||
| chrX:103628898-103629000 | Rare:14 | ||||
| chrX:103629417-103629531 | Common:1; Rare:34 | ||||
| chrX:103686677-103686895 | Common:1; Rare:34 | ||||
| chrX:103688004-103688271 | Common:1; Rare:32 |