Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chrX:135052107-135052369 | Common:2; Rare:68 | ||||
chrX:135344688-135344846 | Rare:32 | ||||
chrX:141177121-141177302 | Rare:24 | ||||
chrX:151397000-151397251 | Common:5; Rare:121 | ||||
chrX:152830712-152831094 | Common:2; Rare:67 | ||||
chrX:153794329-153794684 | Common:1; Rare:109; Clinvar (benign):2 | ||||
chrX:153971181-153971278 | Rare:24 | ||||
chrX:154516179-154516504 | Common:4; Rare:69 | ||||
chrX:154547567-154547639 | Common:1; Rare:16; Clinvar (benign):1 | ||||
chrX:155071105-155071479 | Common:1; Rare:75 | ||||
chrX:155216221-155216480 | Rare:47 |