Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chrX:126471796-126471859 | Rare:16 | ||||
chrX:129984201-129984395 | Rare:17 | ||||
chrX:134413574-134413947 | Common:1; Rare:45; Clinvar:2 | ||||
chrX:134548174-134548402 | Rare:32 | ||||
chrX:134549639-134549761 | Common:1; Rare:33 | ||||
chrX:153506830-153507089 | Common:2; Rare:67 | ||||
chrX:154373621-154373659 | Common:1; Rare:1 | ||||
chrX:154438828-154439091 | Common:1; Rare:58; Clinvar:2; Clinvar (benign):3 | ||||
chrY:2847782-2847997 | |||||
chrY:12662206-12662513 | Rare:3 |