Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:114056475-114056801 | Common:2; Rare:125 | ||||
chr3:119468848-119469010 | Rare:61 | ||||
chr3:120742511-120742766 | Common:2; Rare:70 | ||||
chr3:121749630-121750021 | Common:1; Rare:89 | ||||
chr3:121834987-121835209 | Common:3; Rare:73; Clinvar:6; Clinvar (benign):2 | ||||
chr3:122564264-122564421 | Common:1; Rare:46 | ||||
chr3:123585035-123585164 | Common:1; Rare:49 | ||||
chr3:125375236-125375406 | Rare:47 | ||||
chr3:127598229-127598443 | Common:3; Rare:54 | ||||
chr3:128052139-128052509 | Common:4; Rare:124 | ||||
chr3:129183821-129184091 | Common:2; Rare:95 | ||||
chr3:129249552-129249668 | Common:1; Rare:34 | ||||
chr3:129439924-129440320 | Common:1; Rare:113; Clinvar:1; Clinvar (benign):1 | ||||
chr3:131381531-131381801 | Common:2; Rare:63 | ||||
chr3:132659796-132659890 | Common:3; Rare:21 |