Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:49292562-49292749 | Rare:54 | ||||
chr3:57952317-57952503 | Rare:31 | ||||
chr3:62267333-62267421 | Rare:27 | ||||
chr3:64685046-64685171 | Rare:31 | ||||
chr3:75435092-75435388 | Common:3; Rare:97 | ||||
chr3:75641103-75641291 | Rare:33 | ||||
chr3:80770346-80770630 | Common:5; Rare:48 | ||||
chr3:81761515-81761615 | Common:5; Rare:31; Clinvar (benign):1 | ||||
chr3:88055899-88056118 | Common:1; Rare:53 | ||||
chr3:101576970-101577082 | Common:1; Rare:28 | ||||
chr3:101676275-101676500 | Common:1; Rare:77 | ||||
chr3:101829209-101829232 | Rare:7 | ||||
chr3:104522693-104522770 | Rare:14 | ||||
chr3:105368749-105368773 | Rare:5 | ||||
chr3:107240593-107240764 | Rare:70 |