Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:46069832-46070056 | Rare:47 | ||||
chr3:15738474-15738513 | Rare:10 | ||||
chr3:40453175-40453417 | Common:4; Rare:53 | ||||
chr3:47164775-47164997 | Common:2; Rare:45 | ||||
chr3:75435099-75435388 | Common:3; Rare:95 | ||||
chr3:81761513-81761560 | Common:4; Rare:9; Clinvar (benign):1 | ||||
chr3:101576981-101577102 | Rare:34 | ||||
chr3:101676387-101676500 | Rare:42 | ||||
chr3:107240630-107240824 | Rare:65 | ||||
chr3:130111485-130111778 | Common:3; Rare:69 | ||||
chr3:150408837-150409002 | Rare:49 | ||||
chr3:157174932-157175253 | Common:3; Rare:142 | ||||
chr3:181699317-181699742 | Rare:68 | ||||
chr3:181699751-181699778 | Rare:4 | ||||
chr3:181739940-181740062 | Rare:17 |