Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:677358-677557 | Common:1; Rare:84 | ||||
chr2:3377783-3378080 | Common:2; Rare:94 | ||||
chr2:3558263-3558706 | Common:6; Rare:159 | ||||
chr2:3575095-3575358 | Common:2; Rare:73; Clinvar:3; Clinvar (benign):5 | ||||
chr2:9423393-9423676 | Rare:86 | ||||
chr2:9555765-9556059 | Common:1; Rare:100 | ||||
chr2:9631007-9631346 | Common:3; Rare:100 | ||||
chr2:9843250-9843533 | Common:6; Rare:84 | ||||
chr2:10689925-10689997 | Common:2; Rare:22 | ||||
chr2:12716756-12716954 | Common:1; Rare:51 | ||||
chr2:14632509-14632734 | Rare:82 | ||||
chr2:17753738-17754168 | Common:4; Rare:134; Clinvar (benign):1 | ||||
chr2:19901957-19902019 | Rare:16 | ||||
chr2:19990092-19990229 | Rare:35 | ||||
chr2:20651061-20651260 | Rare:62 |