| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:54440271-54440424 | Rare:25 | ||||
| chrX:54530047-54530296 | Common:2; Rare:35 | ||||
| chrX:55000204-55000425 | Common:1; Rare:52 | ||||
| chrX:55161101-55161276 | Rare:52 | ||||
| chrX:57121476-57121610 | Common:1; Rare:32 | ||||
| chrX:66639076-66639232 | Rare:8 | ||||
| chrX:68433345-68433552 | Rare:31 | ||||
| chrX:68498967-68499056 | Rare:22 | ||||
| chrX:70289875-70290130 | Rare:48 | ||||
| chrX:71532997-71533128 | Rare:17 | ||||
| chrX:74614566-74614886 | Common:1; Rare:75 | ||||
| chrX:77895412-77895750 | Rare:93; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chrX:77899268-77899531 | Rare:65; Clinvar (benign):1 | ||||
| chrX:81201911-81202192 | Rare:51 | ||||
| chrX:100820282-100820419 | Common:2; Rare:29 |