| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:101348678-101348847 | Common:3; Rare:35 | ||||
| chrX:101407814-101408284 | Common:5; Rare:86; Clinvar:2; Clinvar (benign):11 | ||||
| chrX:101622990-101623211 | Common:1; Rare:38 | ||||
| chrX:103215054-103215171 | Common:1; Rare:26 | ||||
| chrX:104156974-104157069 | Rare:15 | ||||
| chrX:108091518-108091818 | Rare:80 | ||||
| chrX:110317946-110318246 | Rare:79 | ||||
| chrX:118345805-118346114 | Common:3; Rare:51 | ||||
| chrX:119574364-119574586 | Rare:50 | ||||
| chrX:119791588-119791986 | Common:2; Rare:105 | ||||
| chrX:119871621-119871914 | Common:2; Rare:61; Clinvar (benign):3 | ||||
| chrX:123961424-123961812 | Rare:48 | ||||
| chrX:129905981-129906201 | Rare:60 | ||||
| chrX:132023160-132023336 | Rare:45 | ||||
| chrX:135052118-135052347 | Common:2; Rare:59 |