Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:42050378-42050534 | Common:1; Rare:47 | ||||
chr6:42879583-42879940 | Rare:103 | ||||
chr6:42929240-42929562 | Common:3; Rare:88 | ||||
chr6:42984309-42984619 | Rare:79 | ||||
chr6:43013869-43014280 | Common:2; Rare:90 | ||||
chr6:43059812-43059853 | Rare:14 | ||||
chr6:43516887-43517102 | Common:3; Rare:83; Clinvar:2 | ||||
chr6:43575962-43576224 | Common:1; Rare:108; Clinvar:7 | ||||
chr6:43770087-43770222 | Common:2; Rare:40 | ||||
chr6:44127351-44127629 | Common:4; Rare:79 | ||||
chr6:47478123-47478173 | Rare:13 | ||||
chr6:49463178-49463407 | Common:1; Rare:68; Clinvar:1; Clinvar (benign):1 | ||||
chr6:52420089-52420356 | Common:3; Rare:114; Clinvar:1; Clinvar (benign):2 | ||||
chr6:52995337-52995713 | Common:4; Rare:150 | ||||
chr6:56542911-56543033 | Common:1; Rare:22 |