Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr8:37849838-37849997 | Common:1; Rare:58 | ||||
chr8:38030278-38030582 | Common:3; Rare:88 | ||||
chr8:38105441-38105556 | Common:1; Rare:42 | ||||
chr8:38105734-38105929 | Rare:63 | ||||
chr8:38176391-38176557 | Common:1; Rare:62 | ||||
chr8:38176674-38176867 | Common:4; Rare:54 | ||||
chr8:38269132-38269256 | Rare:49 | ||||
chr8:38996447-38997049 | Common:7; Rare:229 | ||||
chr8:42338358-42338514 | Common:1; Rare:65 | ||||
chr8:42391797-42391921 | Common:1; Rare:41 | ||||
chr8:42540987-42541173 | Rare:50 | ||||
chr8:42541565-42541661 | Rare:32 | ||||
chr8:42541691-42541854 | Rare:60 | ||||
chr8:42541911-42541980 | Rare:18; Clinvar:1 | ||||
chr8:42843297-42843473 | Common:2; Rare:48; Clinvar (benign):3 |