| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:118345861-118346159 | Common:3; Rare:51 | ||||
| chrX:118495771-118496000 | Common:1; Rare:43 | ||||
| chrX:118727433-118727708 | Rare:61 | ||||
| chrX:118974506-118974653 | Rare:29 | ||||
| chrX:119236551-119236651 | Rare:30 | ||||
| chrX:119468205-119468558 | Common:3; Rare:110 | ||||
| chrX:119469068-119469282 | Rare:62 | ||||
| chrX:119574373-119574603 | Rare:52 | ||||
| chrX:119693378-119693633 | Common:1; Rare:32 | ||||
| chrX:119791578-119791986 | Common:2; Rare:109 | ||||
| chrX:119871622-119872013 | Common:3; Rare:81; Clinvar (benign):4 | ||||
| chrX:120560708-120560865 | Rare:24 | ||||
| chrX:120561420-120561592 | Common:1; Rare:29 | ||||
| chrX:120629934-120630281 | Common:4; Rare:68 | ||||
| chrX:123733009-123733156 | Rare:23; Clinvar (benign):1 |