Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chrX:47210879-47211228 | Rare:70; Clinvar:1; Clinvar (benign):4 | ||||
chrX:47224885-47225098 | Common:1; Rare:32 | ||||
chrX:47366275-47366616 | Common:1; Rare:53 | ||||
chrX:47556158-47556389 | Rare:25 | ||||
chrX:47566727-47567055 | Common:1; Rare:84 | ||||
chrX:49156252-49156448 | Common:2; Rare:48 | ||||
chrX:49230946-49231217 | Common:1; Rare:46 | ||||
chrX:49234158-49234350 | Common:1; Rare:30 | ||||
chrX:49281975-49282598 | Common:1; Rare:87 | ||||
chrX:49879157-49879358 | Rare:31 | ||||
chrX:49881931-49881960 | Common:2; Rare:5 | ||||
chrX:53055142-53055211 | Rare:9 | ||||
chrX:53055864-53056007 | Common:2; Rare:14 | ||||
chrX:53256645-53256714 | Common:2; Rare:10 | ||||
chrX:53405287-53405607 | Rare:41 |