Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:58550224-58550433 | Rare:71 | ||||
chr2:9492898-9493186 | Common:2; Rare:55; Clinvar (benign):2 | ||||
chr2:9495154-9495242 | Rare:12 | ||||
chr2:9495247-9495269 | Rare:4 | ||||
chr2:9495287-9495306 | Rare:6 | ||||
chr2:9999226-9999546 | Common:1; Rare:60 | ||||
chr2:10772283-10772609 | Common:4; Rare:86 | ||||
chr2:10797712-10797848 | Rare:32 | ||||
chr2:15302584-15302866 | Rare:63 | ||||
chr2:19347989-19348177 | Common:1; Rare:71 | ||||
chr2:20207996-20208365 | Common:2; Rare:78 | ||||
chr2:20208466-20208759 | Common:4; Rare:60 | ||||
chr2:20209387-20209642 | Common:1; Rare:50 | ||||
chr2:20211155-20211185 | Rare:5 | ||||
chr2:20212519-20212728 | Rare:45 |