Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:61017440-61017750 | Common:1; Rare:93; Clinvar:2 | ||||
chr2:61144921-61145184 | Common:3; Rare:86 | ||||
chr2:61177203-61177536 | Common:5; Rare:140 | ||||
chr2:61185513-61185534 | Rare:8 | ||||
chr2:61470667-61471033 | Common:1; Rare:120 | ||||
chr2:61471153-61471386 | Common:2; Rare:91 | ||||
chr2:61854000-61854228 | Common:2; Rare:95; Clinvar:1; Clinvar (benign):1 | ||||
chr2:61888515-61888693 | Common:1; Rare:78 | ||||
chr2:62506167-62506330 | Common:1; Rare:57 | ||||
chr2:62706698-62706903 | Rare:36 | ||||
chr2:63588227-63588557 | Common:1; Rare:102; Clinvar:6 | ||||
chr2:63588703-63589040 | Rare:106 | ||||
chr2:63840822-63841165 | Common:2; Rare:94 | ||||
chr2:63841614-63841934 | Common:2; Rare:108 | ||||
chr2:64019395-64019619 | Rare:83 |