Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:138653-138728 | Common:1; Rare:20 | ||||
chr16:234735-234864 | Rare:61 | ||||
chr16:370494-370796 | Common:8; Rare:82 | ||||
chr16:398162-398232 | Common:1; Rare:28 | ||||
chr16:401716-401952 | Common:2; Rare:98 | ||||
chr16:679783-680171 | Common:8; Rare:103 | ||||
chr16:680383-680585 | Common:1; Rare:66 | ||||
chr16:684096-684486 | Common:3; Rare:195 | ||||
chr16:721454-721534 | Rare:22 | ||||
chr16:726843-727149 | Common:5; Rare:77 | ||||
chr16:1351863-1351975 | Common:1; Rare:53; Clinvar:5; Clinvar (benign):1 | ||||
chr16:1771488-1771856 | Common:3; Rare:148 | ||||
chr16:1773106-1773208 | Rare:32 | ||||
chr16:1782507-1783015 | Common:4; Rare:168 | ||||
chr16:1827171-1827225 | Common:1; Rare:26 |