| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:103586435-103586783 | Rare:77 | ||||
| chrX:103607796-103608067 | Rare:48 | ||||
| chrX:103629448-103629531 | Rare:21 | ||||
| chrX:103686660-103686903 | Common:1; Rare:39 | ||||
| chrX:103687015-103687279 | Rare:43 | ||||
| chrX:103688004-103688087 | Rare:18 | ||||
| chrX:104156890-104157070 | Common:1; Rare:29 | ||||
| chrX:106802520-106802787 | Rare:52 | ||||
| chrX:107628269-107628520 | Common:1; Rare:34; Clinvar (benign):1 | ||||
| chrX:107716019-107716401 | Rare:62 | ||||
| chrX:107716427-107716845 | Common:1; Rare:73 | ||||
| chrX:107716929-107717088 | Common:2; Rare:16 | ||||
| chrX:107775606-107775907 | Rare:50 | ||||
| chrX:107775938-107776144 | Common:4; Rare:32 | ||||
| chrX:108091516-108091821 | Rare:80 |