Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:1964704-1965241 | Common:18; Rare:237 | ||||
chr16:1971785-1972141 | Common:3; Rare:108 | ||||
chr16:1983877-1984306 | Common:6; Rare:131; Clinvar (benign):4 | ||||
chr16:1990080-1990444 | Common:2; Rare:68 | ||||
chr16:1991164-1991418 | Rare:53 | ||||
chr16:1991972-1992525 | Common:5; Rare:149 | ||||
chr16:2009254-2009573 | Common:2; Rare:91 | ||||
chr16:2009734-2010049 | Common:14; Rare:119 | ||||
chr16:2047769-2048056 | Rare:142; Clinvar:2; Clinvar (benign):4 | ||||
chr16:2135882-2136158 | Common:1; Rare:131; Clinvar (benign):1 | ||||
chr16:2155218-2155850 | Common:2; Rare:213 | ||||
chr16:2205149-2205569 | Common:3; Rare:113 | ||||
chr16:2205608-2205947 | Common:5; Rare:152 | ||||
chr16:2214727-2215172 | Common:3; Rare:170 | ||||
chr16:2215223-2215435 | Common:1; Rare:56 |