Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:45595947-45596038 | Rare:30 | ||||
chr3:49357222-49357339 | Rare:32 | ||||
chr3:62149994-62150170 | Rare:38 | ||||
chr3:98981101-98981387 | Common:2; Rare:40 | ||||
chr3:107240600-107240724 | Rare:52 | ||||
chr3:112640166-112640528 | Common:1; Rare:60 | ||||
chr3:153164018-153164055 | Rare:4 | ||||
chr3:160515233-160515477 | Common:1; Rare:47 | ||||
chr3:169765058-169765182 | Rare:56; Clinvar (pathogenic):1 | ||||
chr3:170726680-170726862 | Rare:31 | ||||
chr3:184317465-184317808 | Common:2; Rare:89 | ||||
chr3:184323498-184323809 | Common:3; Rare:78 | ||||
chr4:6673867-6674077 | Common:11; Rare:99 | ||||
chr4:68376590-68376627 | Rare:5 | ||||
chr4:73998011-73998153 | Rare:47 |