| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:111681162-111681302 | Rare:41; Clinvar (benign):7 | ||||
| chrX:112840581-112840682 | Rare:16 | ||||
| chrX:112840770-112841010 | Rare:49 | ||||
| chrX:115560987-115561244 | Common:1; Rare:47 | ||||
| chrX:118116655-118116929 | Common:1; Rare:44 | ||||
| chrX:118345832-118346133 | Common:3; Rare:53 | ||||
| chrX:119236514-119236685 | Rare:45 | ||||
| chrX:119468216-119468517 | Common:3; Rare:101 | ||||
| chrX:119469090-119469260 | Rare:49 | ||||
| chrX:119574356-119574586 | Rare:50 | ||||
| chrX:119605853-119606141 | Rare:41 | ||||
| chrX:119693104-119693404 | Common:2; Rare:67 | ||||
| chrX:119791572-119791994 | Common:2; Rare:112 | ||||
| chrX:119852930-119853256 | Common:3; Rare:53; Clinvar (benign):3 | ||||
| chrX:119871621-119871947 | Common:2; Rare:68; Clinvar (benign):3 |