| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:101348660-101348956 | Common:4; Rare:66; Clinvar:1; Clinvar (benign):2 | ||||
| chrX:101354564-101354691 | Rare:13 | ||||
| chrX:101390766-101391021 | Rare:62 | ||||
| chrX:101407777-101408288 | Common:5; Rare:92; Clinvar:2; Clinvar (benign):12 | ||||
| chrX:101617888-101618049 | Common:1; Rare:33 | ||||
| chrX:104156978-104157063 | Rare:14 | ||||
| chrX:107716771-107716784 | Rare:1 | ||||
| chrX:107716811-107717193 | Common:2; Rare:53 | ||||
| chrX:108091450-108091822 | Rare:97 | ||||
| chrX:111680984-111681234 | Rare:62; Clinvar (benign):5 | ||||
| chrX:118727402-118727717 | Common:1; Rare:73 | ||||
| chrX:119468216-119468475 | Common:3; Rare:80 | ||||
| chrX:119469056-119469233 | Rare:51 | ||||
| chrX:119574412-119574581 | Rare:38 | ||||
| chrX:119758426-119758622 | Common:2; Rare:32 |