| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:70289888-70290122 | Rare:43 | ||||
| chrX:71532894-71533111 | Rare:43 | ||||
| chrX:75156273-75156388 | Common:2; Rare:28 | ||||
| chrX:78103962-78104304 | Common:4; Rare:122 | ||||
| chrX:81201876-81202031 | Rare:26 | ||||
| chrX:81202043-81202147 | Rare:13 | ||||
| chrX:101348728-101348805 | Common:2; Rare:10 | ||||
| chrX:101407893-101408248 | Common:5; Rare:65; Clinvar:1; Clinvar (benign):10 | ||||
| chrX:104156955-104157063 | Common:1; Rare:18 | ||||
| chrX:108091529-108091796 | Rare:69 | ||||
| chrX:109733185-109733491 | Common:1; Rare:72 | ||||
| chrX:119574374-119574568 | Rare:43 | ||||
| chrX:119791590-119791714 | Rare:49 | ||||
| chrX:119871673-119871921 | Common:1; Rare:56; Clinvar (benign):3 | ||||
| chrX:129843794-129844068 | Common:1; Rare:36 |