Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:980741-981093 | Common:5; Rare:96 | ||||
chr16:1420728-1420941 | Common:1; Rare:86 | ||||
chr16:1678048-1678321 | Common:3; Rare:90 | ||||
chr16:1706069-1706353 | Common:2; Rare:89 | ||||
chr16:1771515-1771835 | Common:3; Rare:124 | ||||
chr16:1773082-1773213 | Rare:44 | ||||
chr16:1782646-1783009 | Common:1; Rare:113 | ||||
chr16:1826800-1826915 | Common:1; Rare:35 | ||||
chr16:1959404-1959643 | Common:5; Rare:105 | ||||
chr16:1964821-1964944 | Common:4; Rare:44 | ||||
chr16:1971904-1972106 | Common:1; Rare:58 | ||||
chr16:2009637-2009896 | Common:15; Rare:103 | ||||
chr16:2047813-2048033 | Rare:99; Clinvar:2; Clinvar (benign):1 | ||||
chr16:2155350-2155654 | Rare:89 | ||||
chr16:2223304-2223628 | Rare:128 |