Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:123700927-123701308 | Common:1; Rare:81; Clinvar:4; Clinvar (benign):2 | ||||
chr3:123961194-123961531 | Common:3; Rare:131 | ||||
chr3:124730378-124730474 | Common:2; Rare:53; Clinvar:2; Clinvar (benign):2 | ||||
chr3:125375231-125375422 | Rare:56 | ||||
chr3:127598212-127598458 | Common:3; Rare:73 | ||||
chr3:127628965-127629227 | Common:1; Rare:89 | ||||
chr3:127672824-127673007 | Common:1; Rare:87 | ||||
chr3:127822426-127822747 | Common:1; Rare:70 | ||||
chr3:127823175-127823369 | Common:3; Rare:40 | ||||
chr3:128052170-128052532 | Common:2; Rare:122 | ||||
chr3:128680633-128680883 | Common:3; Rare:76 | ||||
chr3:128726057-128726225 | Common:1; Rare:45; Clinvar:3 | ||||
chr3:128879425-128879675 | Common:4; Rare:123; Clinvar:2; Clinvar (benign):2 | ||||
chr3:129161004-129161123 | Rare:48 | ||||
chr3:129183788-129184079 | Common:2; Rare:97 |