| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:109733171-109733500 | Common:1; Rare:78 | ||||
| chrX:110318072-110318310 | Rare:71 | ||||
| chrX:118345885-118346187 | Common:3; Rare:55 | ||||
| chrX:118974497-118974653 | Rare:29 | ||||
| chrX:119236108-119236390 | Rare:75 | ||||
| chrX:119236575-119236651 | Rare:20 | ||||
| chrX:119468205-119468572 | Common:3; Rare:111 | ||||
| chrX:119469090-119469282 | Rare:56 | ||||
| chrX:119574364-119574592 | Rare:51 | ||||
| chrX:119791577-119791978 | Common:2; Rare:108 | ||||
| chrX:119852924-119853276 | Common:3; Rare:57; Clinvar (benign):3 | ||||
| chrX:119871605-119871969 | Common:2; Rare:71; Clinvar (benign):3 | ||||
| chrX:119943595-119943852 | Rare:45 | ||||
| chrX:120250660-120250905 | Common:3; Rare:41 | ||||
| chrX:120560726-120560859 | Rare:19 |