Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:61362278-61362404 | Common:1; Rare:36; Clinvar:6 | ||||
chr11:61392487-61392649 | Common:2; Rare:53; Clinvar:4; Clinvar (benign):2 | ||||
chr11:61429904-61430144 | Common:1; Rare:104; Clinvar (benign):2 | ||||
chr11:61792573-61792947 | Common:5; Rare:99 | ||||
chr11:61816764-61816971 | Rare:63 | ||||
chr11:61917410-61917658 | Common:2; Rare:86 | ||||
chr11:61967312-61967807 | Common:3; Rare:185; Clinvar:4 | ||||
chr11:62545606-62545931 | Common:1; Rare:68 | ||||
chr11:62546637-62546925 | Common:1; Rare:87 | ||||
chr11:62591495-62591823 | Rare:109 | ||||
chr11:62611448-62611841 | Rare:103 | ||||
chr11:62621931-62622234 | Common:2; Rare:94 | ||||
chr11:62665165-62665452 | Common:6; Rare:131 | ||||
chr11:62678866-62679175 | Rare:103 | ||||
chr11:62706238-62706405 | Common:2; Rare:72; Clinvar (benign):4 |