| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:102516665-102517014 | Common:3; Rare:43 | ||||
| chrX:103064094-103064503 | Common:3; Rare:62 | ||||
| chrX:103215011-103215309 | Common:2; Rare:51 | ||||
| chrX:103310870-103311148 | Common:2; Rare:37 | ||||
| chrX:103376412-103376607 | Common:1; Rare:31 | ||||
| chrX:103585451-103585586 | Common:2; Rare:32 | ||||
| chrX:103586476-103586678 | Rare:40 | ||||
| chrX:103686667-103687003 | Common:4; Rare:44 | ||||
| chrX:104156974-104157078 | Rare:16 | ||||
| chrX:107717060-107717156 | Rare:14 | ||||
| chrX:108091500-108091815 | Rare:86 | ||||
| chrX:110318077-110318251 | Rare:43 | ||||
| chrX:111680964-111681205 | Rare:49; Clinvar (benign):1 | ||||
| chrX:111681552-111681753 | Rare:68 | ||||
| chrX:115560987-115561243 | Common:1; Rare:47 |