Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:15561297-15561353 | Rare:31 | ||||
chr2:15940337-15940774 | Common:2; Rare:108 | ||||
chr2:17539919-17540007 | Rare:18 | ||||
chr2:17540455-17540842 | Common:2; Rare:81 | ||||
chr2:17753711-17754195 | Common:5; Rare:150; Clinvar (benign):1 | ||||
chr2:18560597-18560805 | Rare:64 | ||||
chr2:19901628-19901761 | Common:1; Rare:71 | ||||
chr2:19901945-19902051 | Common:1; Rare:35 | ||||
chr2:19989595-19989738 | Rare:24 | ||||
chr2:19990036-19990213 | Rare:48 | ||||
chr2:20051524-20051878 | Common:1; Rare:98 | ||||
chr2:20225025-20225278 | Common:1; Rare:68 | ||||
chr2:20225724-20225749 | Common:2; Rare:6 | ||||
chr2:20350625-20350927 | Common:1; Rare:98 | ||||
chr2:20446841-20447086 | Common:3; Rare:103 |