| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:104156899-104157078 | Common:1; Rare:30 | ||||
| chrX:106802520-106802763 | Rare:51 | ||||
| chrX:107628269-107628517 | Common:1; Rare:34; Clinvar (benign):1 | ||||
| chrX:108091516-108091823 | Rare:82 | ||||
| chrX:108439447-108439864 | Common:2; Rare:95 | ||||
| chrX:109537065-109537254 | Common:1; Rare:40 | ||||
| chrX:109733167-109733511 | Common:1; Rare:83 | ||||
| chrX:110318072-110318251 | Rare:46 | ||||
| chrX:118345832-118346174 | Common:4; Rare:61 | ||||
| chrX:119468216-119468533 | Common:3; Rare:104 | ||||
| chrX:119565352-119565533 | Common:3; Rare:39 | ||||
| chrX:119791573-119791994 | Common:2; Rare:112 | ||||
| chrX:119852939-119853306 | Common:4; Rare:61; Clinvar (benign):3 | ||||
| chrX:119871603-119871923 | Common:2; Rare:63; Clinvar (benign):3 | ||||
| chrX:119943559-119943840 | Rare:58 |