Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chrX:15675636-15675735 | Common:1; Rare:19 | ||||
chrX:23679038-23679277 | Rare:51 | ||||
chrX:45746722-45746751 | Rare:3 | ||||
chrX:47196486-47196593 | Rare:11 | ||||
chrX:55452866-55453146 | Rare:60 | ||||
chrX:56564243-56564330 | Rare:18 | ||||
chrX:56564572-56564873 | Common:1; Rare:47 | ||||
chrX:65736893-65737354 | Common:1; Rare:87 | ||||
chrX:67545608-67545701 | Rare:20; Clinvar (pathogenic):1 | ||||
chrX:74292481-74292742 | Rare:43 | ||||
chrX:77599555-77599746 | Common:1; Rare:40; Clinvar:1; Clinvar (benign):2 | ||||
chrX:78113858-78114157 | Rare:80; Clinvar:2 | ||||
chrX:108087808-108088093 | Rare:53 | ||||
chrX:109732155-109732587 | Rare:63 | ||||
chrX:119851530-119851779 | Common:5; Rare:39; Clinvar (benign):1 |