Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:47335195-47335324 | Rare:29 | ||||
chr2:47691278-47691560 | Common:4; Rare:51 | ||||
chr2:47798503-47798678 | Common:2; Rare:73; Clinvar:20; Clinvar (benign):14; Clinvar (pathogenic):2 | ||||
chr2:47904390-47904470 | Rare:19 | ||||
chr2:47906392-47906861 | Common:2; Rare:173 | ||||
chr2:47907319-47907387 | Rare:15 | ||||
chr2:48397897-48398084 | Common:1; Rare:33 | ||||
chr2:48398316-48398487 | Rare:38 | ||||
chr2:50922665-50922815 | Rare:47; Clinvar:2; Clinvar (benign):1 | ||||
chr2:54629764-54630027 | Common:2; Rare:63 | ||||
chr2:56049634-56049800 | Rare:36 | ||||
chr2:58428202-58428443 | Common:3; Rare:80 | ||||
chr2:58429155-58429340 | Rare:45 | ||||
chr2:58913057-58913321 | Rare:54 | ||||
chr2:59080438-59080666 | Common:1; Rare:40 |