Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:26672956-26673104 | Common:1; Rare:50 | ||||
chr22:27473606-27473863 | Common:2; Rare:55 | ||||
chr22:28799396-28799528 | Rare:27 | ||||
chr22:30969035-30969302 | Common:2; Rare:77 | ||||
chr22:36288725-36289301 | Common:2; Rare:174; Clinvar:6; Clinvar (benign):10 | ||||
chr22:38336179-38336288 | Rare:29 | ||||
chr22:39521555-39521813 | Common:1; Rare:126 | ||||
chr22:46052808-46052928 | Rare:27 | ||||
chr22:46069827-46070067 | Rare:50 | ||||
chr22:50757207-50757221 | Rare:2 | ||||
chr3:4978311-4978575 | Common:2; Rare:77 | ||||
chr3:9396249-9396325 | Rare:36 | ||||
chr3:40453163-40453402 | Common:6; Rare:53 | ||||
chr3:48579497-48579794 | Common:1; Rare:81; Clinvar:2; Clinvar (pathogenic):1 | ||||
chr3:48581120-48581271 | Common:1; Rare:46; Clinvar:1; Clinvar (pathogenic):2 |