| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:111681941-111682183 | Common:1; Rare:41; Clinvar (benign):2 | ||||
| chrX:112840863-112841033 | Rare:32 | ||||
| chrX:115189240-115189431 | Common:1; Rare:41 | ||||
| chrX:115289505-115289762 | Common:2; Rare:79 | ||||
| chrX:115561046-115561225 | Common:1; Rare:27 | ||||
| chrX:116462964-116463141 | Rare:25 | ||||
| chrX:118116765-118116933 | Common:1; Rare:25 | ||||
| chrX:118345853-118346191 | Common:3; Rare:60 | ||||
| chrX:119073712-119073781 | Rare:12 | ||||
| chrX:119235939-119236379 | Rare:102 | ||||
| chrX:119236559-119236651 | Rare:26 | ||||
| chrX:119468167-119468554 | Common:4; Rare:118 | ||||
| chrX:119469040-119469148 | Rare:28 | ||||
| chrX:119574356-119574592 | Rare:51 | ||||
| chrX:119693074-119693485 | Common:3; Rare:88 |