Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:19352995-19353169 | Common:3; Rare:35 | ||||
chr2:19364081-19364267 | Rare:40 | ||||
chr2:20447729-20448326 | Rare:189 | ||||
chr2:20448331-20448909 | Common:4; Rare:150 | ||||
chr2:20450931-20450967 | Rare:12 | ||||
chr2:20501318-20501553 | Common:19; Rare:98 | ||||
chr2:23467400-23467650 | Rare:35 | ||||
chr2:23925872-23926145 | Common:1; Rare:55 | ||||
chr2:24830707-24830913 | Rare:60 | ||||
chr2:24873696-24873953 | Common:2; Rare:50 | ||||
chr2:25822050-25822349 | Common:6; Rare:62 | ||||
chr2:26191487-26191765 | Common:1; Rare:81; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr2:26204131-26204443 | Rare:51; Clinvar (pathogenic):1 | ||||
chr2:27185196-27185471 | Common:2; Rare:49 | ||||
chr2:27375684-27375970 | Common:1; Rare:114 |