Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:107926348-107926706 | Common:2; Rare:80; Clinvar (benign):1 | ||||
chr7:107944672-107944731 | Common:1; Rare:11 | ||||
chr7:107947101-107947453 | Common:1; Rare:76 | ||||
chr7:107951214-107951526 | Common:3; Rare:84; Clinvar (benign):2 | ||||
chr7:111226280-111226331 | Rare:11 | ||||
chr7:111413870-111413985 | Rare:25 | ||||
chr7:111421393-111421434 | Common:1; Rare:6 | ||||
chr7:111439371-111439539 | Rare:27 | ||||
chr7:111458729-111458847 | Rare:22 | ||||
chr7:122116665-122116888 | Rare:66 | ||||
chr7:128454494-128454674 | Common:1; Rare:40 | ||||
chr7:130536509-130536781 | Common:3; Rare:65 | ||||
chr7:130913572-130913652 | Rare:20 | ||||
chr7:130930433-130930573 | Common:1; Rare:22 | ||||
chr7:130941486-130941699 | Common:1; Rare:30 |