Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chrX:11111141-11111356 | Common:3; Rare:45 | ||||
chrX:13734584-13734815 | Common:3; Rare:73; Clinvar (benign):1 | ||||
chrX:14873035-14873362 | Common:1; Rare:61 | ||||
chrX:15335536-15335835 | Common:3; Rare:60 | ||||
chrX:47145058-47145273 | Rare:33 | ||||
chrX:53422645-53422786 | Rare:34 | ||||
chrX:54530021-54530246 | Common:4; Rare:33 | ||||
chrX:68498981-68499059 | Rare:16 | ||||
chrX:70289875-70290122 | Rare:47 | ||||
chrX:74614574-74614870 | Common:1; Rare:69 | ||||
chrX:77899258-77899505 | Rare:57 | ||||
chrX:81201887-81202192 | Rare:52 | ||||
chrX:101390794-101391036 | Rare:67 | ||||
chrX:101407897-101408264 | Common:5; Rare:65; Clinvar (benign):9 | ||||
chrX:108091513-108091818 | Rare:80 |