Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chrX:15675574-15675782 | Common:2; Rare:47 | ||||
chrX:15728651-15728680 | Rare:1 | ||||
chrX:15836606-15836835 | Common:1; Rare:36 | ||||
chrX:16156228-16156480 | Common:2; Rare:24 | ||||
chrX:16156852-16156884 | Rare:1 | ||||
chrX:16215785-16216058 | Common:2; Rare:38 | ||||
chrX:16577138-16577225 | Common:1; Rare:10 | ||||
chrX:16591800-16591878 | Rare:6 | ||||
chrX:16832452-16832743 | Common:1; Rare:39 | ||||
chrX:18355255-18355350 | Rare:8 | ||||
chrX:19349703-19350016 | Common:2; Rare:37; Clinvar (benign):1 | ||||
chrX:23349052-23349119 | Rare:7 | ||||
chrX:23349284-23349465 | Common:2; Rare:24 | ||||
chrX:23422505-23422583 | Common:1; Rare:10 | ||||
chrX:24025278-24025468 | Common:2; Rare:46 |