Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:49278035-49278256 | Rare:58 | ||||
chr20:49278421-49278665 | Common:8; Rare:84 | ||||
chr20:49568093-49568418 | Common:11; Rare:75 | ||||
chr20:50113135-50113244 | Common:5; Rare:54 | ||||
chr20:50958497-50958872 | Common:1; Rare:132; Clinvar:1; Clinvar (benign):3 | ||||
chr20:56392187-56392704 | Common:6; Rare:137 | ||||
chr20:57709958-57710192 | Rare:66 | ||||
chr20:57710547-57710753 | Common:1; Rare:57 | ||||
chr20:58309418-58309731 | Common:2; Rare:119 | ||||
chr20:58515397-58515521 | Common:2; Rare:22 | ||||
chr20:58651529-58651832 | Common:1; Rare:73; Clinvar:2; Clinvar (benign):3 | ||||
chr20:58891320-58891648 | Common:1; Rare:133; Clinvar:2 | ||||
chr20:58909165-58909412 | Common:3; Rare:56; Clinvar:1; Clinvar (pathogenic):2 | ||||
chr20:58910046-58910399 | Rare:90 | ||||
chr20:58981178-58981323 | Common:2; Rare:79 |