Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chrX:120604061-120604152 | Rare:22 | ||||
chrX:123733025-123733152 | Rare:20 | ||||
chrX:123960350-123960731 | Rare:28 | ||||
chrX:123961264-123961432 | Common:2; Rare:22 | ||||
chrX:123961514-123961837 | Rare:45 | ||||
chrX:124346461-124346563 | Rare:7; Clinvar (benign):1 | ||||
chrX:129779833-129779980 | Rare:22 | ||||
chrX:129906041-129906201 | Rare:43 | ||||
chrX:132023168-132023336 | Rare:43 | ||||
chrX:132217719-132218308 | Common:1; Rare:74 | ||||
chrX:135344654-135344830 | Rare:36 | ||||
chrX:135973731-135973879 | Rare:47 | ||||
chrX:141177056-141177309 | Common:1; Rare:35 | ||||
chrX:145817582-145817928 | Common:2; Rare:60 | ||||
chrX:149540422-149540753 | Common:2; Rare:45 |