| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:107716438-107716565 | Common:1; Rare:22 | ||||
| chrX:107717058-107717192 | Rare:18 | ||||
| chrX:108091516-108091784 | Rare:70 | ||||
| chrX:108439486-108440006 | Common:3; Rare:112 | ||||
| chrX:108736318-108736561 | Rare:42 | ||||
| chrX:109536548-109536887 | Common:1; Rare:43 | ||||
| chrX:109537065-109537256 | Common:1; Rare:40 | ||||
| chrX:111681536-111681757 | Rare:75 | ||||
| chrX:118345859-118346155 | Common:3; Rare:50 | ||||
| chrX:119236575-119236624 | Rare:11 | ||||
| chrX:119468205-119468506 | Common:3; Rare:99 | ||||
| chrX:119565354-119565485 | Common:3; Rare:32 | ||||
| chrX:119574395-119574586 | Rare:40 | ||||
| chrX:119791590-119791753 | Common:2; Rare:63 | ||||
| chrX:119871670-119871904 | Common:1; Rare:54; Clinvar (benign):2 |