| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:107628266-107628536 | Common:1; Rare:37; Clinvar (benign):1 | ||||
| chrX:107716414-107716851 | Common:1; Rare:76 | ||||
| chrX:108091500-108091818 | Rare:86 | ||||
| chrX:109536539-109536866 | Common:1; Rare:39 | ||||
| chrX:109733177-109733536 | Common:1; Rare:83 | ||||
| chrX:110318077-110318229 | Rare:36 | ||||
| chrX:111096009-111096194 | Rare:27 | ||||
| chrX:111681014-111681313 | Rare:76; Clinvar (benign):7 | ||||
| chrX:111681536-111681705 | Rare:63 | ||||
| chrX:112840775-112841048 | Rare:55 | ||||
| chrX:115561100-115561244 | Common:1; Rare:26 | ||||
| chrX:118116750-118116870 | Rare:17 | ||||
| chrX:119236473-119236626 | Rare:46 | ||||
| chrX:119468205-119468512 | Common:3; Rare:102 | ||||
| chrX:119565353-119565504 | Common:3; Rare:34 |