Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:127598219-127598456 | Common:3; Rare:68 | ||||
chr3:127823180-127823340 | Common:3; Rare:31 | ||||
chr3:128052194-128052532 | Common:2; Rare:111 | ||||
chr3:128153324-128153496 | Common:2; Rare:46 | ||||
chr3:128680633-128680799 | Common:2; Rare:47 | ||||
chr3:128726056-128726225 | Common:1; Rare:46; Clinvar:3 | ||||
chr3:128879435-128879669 | Common:4; Rare:116; Clinvar:2; Clinvar (benign):2 | ||||
chr3:129183805-129184051 | Common:2; Rare:80 | ||||
chr3:129249536-129249668 | Common:1; Rare:38 | ||||
chr3:129278761-129278895 | Common:4; Rare:43 | ||||
chr3:129439876-129440340 | Common:1; Rare:143; Clinvar:2; Clinvar (benign):1 | ||||
chr3:129893592-129893882 | Rare:128 | ||||
chr3:130893885-130894265 | Common:3; Rare:117 | ||||
chr3:131026772-131026942 | Common:2; Rare:39 | ||||
chr3:131381487-131381801 | Common:2; Rare:78 |