chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
168152370681523707GA12GENIChomozygous125676180
168152426081524261TC19GENIChomozygous125676182
168152436381524364GA31GENIChomozygous125676184
168152575781525758AG20GENIChomozygous125676186
168152643381526434CA18GENIChomozygous125676188
168152650981526510TC20GENIChomozygous125676190
168152658481526585AG9GENIChomozygous125676192
168152658681526587AT7GENIChomozygous125676194
168152700581527006AG7GENIChomozygous125676196
168152766481527665AG19GENIChomozygous125676198
168152778081527781GA14GENIChomozygous125676200
168152910381529104AG6GENIChomozygous125676202
168152910481529105CG6GENIChomozygous125676204
168153021481530215GA18GENIChomozygous125676206
168153022981530230CG16GENIChomozygous125676208
168153102481531025AG10GENIChomozygous125676210
168153103081531031GA10GENIChomozygous125676212
168153126781531268CA7GENIChomozygous125676214
168153165581531656TC12GENIChomozygous125676216
168153181381531814TC19GENIChomozygous125676218
168153196581531966CT16GENIChomozygous125676220