Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr8:30744108-30744430 | Common:3; Rare:106 | ||||
chr8:33484886-33485204 | Common:8; Rare:102 | ||||
chr8:37762478-37762672 | Common:2; Rare:68 | ||||
chr8:38030259-38030632 | Common:3; Rare:108 | ||||
chr8:38105356-38105559 | Common:2; Rare:62 | ||||
chr8:38176430-38176542 | Common:1; Rare:40 | ||||
chr8:38176680-38176863 | Common:2; Rare:50 | ||||
chr8:38996443-38997042 | Common:7; Rare:228 | ||||
chr8:40153358-40153502 | Common:1; Rare:35 | ||||
chr8:42540882-42541178 | Rare:76 | ||||
chr8:42541557-42541666 | Rare:36 | ||||
chr8:42541674-42541965 | Common:1; Rare:94; Clinvar:1; Clinvar (benign):1 | ||||
chr8:42843290-42843467 | Common:2; Rare:45; Clinvar (benign):3 | ||||
chr8:43056115-43056463 | Common:1; Rare:124 | ||||
chr8:47260746-47260981 | Common:3; Rare:105 |