| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:38561281-38561549 | Common:3; Rare:69; Clinvar (benign):1 | ||||
| chrX:47144684-47144815 | Common:1; Rare:20 | ||||
| chrX:48475897-48476247 | Rare:61 | ||||
| chrX:48508881-48509043 | Rare:32 | ||||
| chrX:56729434-56729535 | Common:1; Rare:11 | ||||
| chrX:57121475-57121678 | Common:1; Rare:48 | ||||
| chrX:68498965-68499057 | Rare:22 | ||||
| chrX:70289875-70290093 | Rare:41 | ||||
| chrX:77895419-77895736 | Rare:84; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chrX:81201887-81202128 | Rare:41 | ||||
| chrX:101407923-101408274 | Common:3; Rare:59; Clinvar (benign):5 | ||||
| chrX:103356444-103356557 | Common:2; Rare:14 | ||||
| chrX:108091447-108091818 | Rare:96 | ||||
| chrX:119871680-119871884 | Common:1; Rare:48; Clinvar (benign):2 | ||||
| chrX:123733006-123733189 | Rare:34; Clinvar (benign):1 |