Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chrX:1392066-1392395 | Common:6; Rare:143 | ||||
chrX:7927379-7927512 | Common:1; Rare:33 | ||||
chrX:7927697-7927758 | Rare:10 | ||||
chrX:10156861-10157021 | Rare:19 | ||||
chrX:10620458-10620688 | Common:1; Rare:31 | ||||
chrX:11111136-11111359 | Common:3; Rare:48 | ||||
chrX:12976136-12976195 | Rare:9 | ||||
chrX:13688969-13689188 | Rare:55 | ||||
chrX:13734540-13734815 | Common:3; Rare:87; Clinvar (benign):1 | ||||
chrX:14873200-14873470 | Rare:45 | ||||
chrX:16719463-16719690 | Rare:67 | ||||
chrX:16786163-16786490 | Common:2; Rare:66 | ||||
chrX:21940640-21940806 | Common:2; Rare:44 | ||||
chrX:23667361-23667576 | Common:2; Rare:68 | ||||
chrX:23783043-23783220 | Common:3; Rare:33 |