Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr18:59899818-59900040 | Common:3; Rare:73 | ||||
chr18:62186960-62187285 | Common:4; Rare:87 | ||||
chr18:62526736-62526860 | Common:2; Rare:61 | ||||
chr18:63367198-63367316 | Rare:40 | ||||
chr18:68715009-68715271 | Common:5; Rare:116 | ||||
chr18:70205672-70205803 | Common:3; Rare:48; Clinvar (benign):2 | ||||
chr18:74597583-74597892 | Common:2; Rare:83 | ||||
chr18:77132741-77132790 | Rare:14 | ||||
chr18:79400073-79400344 | Common:4; Rare:89 | ||||
chr18:79679485-79679922 | Common:5; Rare:175 | ||||
chr18:79988413-79988675 | Common:4; Rare:100; Clinvar (pathogenic):2 | ||||
chr19:572240-572610 | Common:3; Rare:177 | ||||
chr19:633510-633752 | Common:8; Rare:111 | ||||
chr19:663143-663445 | Common:2; Rare:123 | ||||
chr19:680486-680783 | Common:2; Rare:104 |