Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chrX:77895412-77895741 | Rare:92; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chrX:78103951-78104298 | Common:4; Rare:125 | ||||
chrX:80335349-80335404 | Common:1; Rare:8 | ||||
chrX:81201876-81202229 | Rare:57 | ||||
chrX:100644128-100644263 | Common:1; Rare:19 | ||||
chrX:101407897-101408282 | Common:5; Rare:69; Clinvar (benign):9 | ||||
chrX:101418225-101418351 | Common:1; Rare:20 | ||||
chrX:102651296-102651523 | Common:2; Rare:65 | ||||
chrX:103214993-103215177 | Common:2; Rare:39 | ||||
chrX:103586435-103586743 | Rare:67 | ||||
chrX:103607665-103608036 | Common:1; Rare:60 | ||||
chrX:103629448-103629520 | Rare:19 | ||||
chrX:103686671-103687029 | Common:4; Rare:48 | ||||
chrX:103687176-103687284 | Rare:22 | ||||
chrX:104156899-104157078 | Common:1; Rare:30 |