Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:14959428-14959609 | Rare:34 | ||||
chr3:15257164-15257251 | Common:1; Rare:20 | ||||
chr3:15258614-15258856 | Rare:66 | ||||
chr3:15261167-15261418 | Common:1; Rare:48 | ||||
chr3:15738245-15738634 | Common:3; Rare:87 | ||||
chr3:24162764-24162779 | Rare:3 | ||||
chr3:37916184-37916483 | Common:1; Rare:56 | ||||
chr3:38455420-38455460 | Common:1; Rare:12 | ||||
chr3:39384289-39384488 | Common:4; Rare:44 | ||||
chr3:40077288-40077387 | Rare:19 | ||||
chr3:40453163-40453435 | Common:6; Rare:61 | ||||
chr3:41225506-41225727 | Rare:44; Clinvar (pathogenic):1 | ||||
chr3:41233193-41233407 | Common:1; Rare:37 | ||||
chr3:43326361-43326498 | Common:1; Rare:27 | ||||
chr3:43339380-43339535 | Common:1; Rare:21 |