Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:4614835-4615080 | Common:1; Rare:70 | ||||
chr16:4734179-4734558 | Common:1; Rare:127 | ||||
chr16:4847244-4847573 | Common:3; Rare:155 | ||||
chr16:4893262-4893466 | Rare:79 | ||||
chr16:5033920-5033968 | Rare:19 | ||||
chr16:5097735-5098004 | Common:4; Rare:99 | ||||
chr16:8674396-8674663 | Common:1; Rare:98; Clinvar:2 | ||||
chr16:8797621-8797877 | Rare:101; Clinvar:2; Clinvar (benign):2 | ||||
chr16:10580569-10580855 | Common:2; Rare:96 | ||||
chr16:10944327-10944645 | Common:1; Rare:100 | ||||
chr16:11742821-11743016 | Common:2; Rare:74 | ||||
chr16:11797176-11797543 | Common:4; Rare:143 | ||||
chr16:11851406-11851672 | Common:1; Rare:139 | ||||
chr16:11915372-11915727 | Common:5; Rare:136 | ||||
chr16:11915893-11916208 | Common:2; Rare:129 |