Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:60881326-60881657 | Common:2; Rare:130 | ||||
chr2:61017419-61017756 | Common:1; Rare:102; Clinvar:2; Clinvar (benign):2 | ||||
chr2:61144926-61145165 | Common:3; Rare:79 | ||||
chr2:61470651-61470991 | Rare:112 | ||||
chr2:61471167-61471386 | Common:2; Rare:83 | ||||
chr2:61536584-61536767 | Common:1; Rare:54 | ||||
chr2:61854037-61854223 | Common:2; Rare:72; Clinvar:1; Clinvar (benign):1 | ||||
chr2:61888509-61888707 | Common:1; Rare:83 | ||||
chr2:63588914-63589040 | Rare:45 | ||||
chr2:63840804-63841185 | Common:3; Rare:108 | ||||
chr2:63841842-63841984 | Common:1; Rare:43 | ||||
chr2:63842178-63842251 | Rare:29 | ||||
chr2:63842252-63842507 | Rare:82 | ||||
chr2:64524137-64524393 | Common:1; Rare:74 | ||||
chr2:64988449-64988516 | Rare:15 |