chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
84967728649677287GA21GENIChomozygous116489227
84967886849678869CT18GENIChomozygous116489229
84967895649678957TC21GENIChomozygous116489231
84967902749679028TC21GENIChomozygous116489233
84967912249679123CA37GENIChomozygous116489235
84967962449679625CT29GENIChomozygous116489237
84968088349680884CT29GENIChomozygous116489241
84968216449682165TC20GENIChomozygous116489245
84968297949682980AG15GENIChomozygous116489247
84968324549683246TG17GENIChomozygous116489249
84968465449684655GA50GENIChomozygous116489251
84968473549684736GA39GENIChomozygous116489253
84968476249684763TC38GENIChomozygous116489255
84968602249686023GC29GENIChomozygous116489257
84968698549686986TG27GENIChomozygous116489259
84968724449687245GA27GENIChomozygous116489261
84968751049687511GC29GENIChomozygous116489263
84968755949687560CT32GENIChomozygous116489265
84968779349687794GT37GENIChomozygous116489267
84968939249689393CT28GENIChomozygous116489269
84969031249690313AG19GENIChomozygous116489271
84969104949691050GA19GENIChomozygous116489275
84969161549691616AC17GENIChomozygous116489277
84969183749691838AG25GENIChomozygous116489283
84969217149692172GA30GENIChomozygous116489285
84969240449692405TC29GENIChomozygous116489287
84969298449692985AG18GENIChomozygous116489289
84969397049693971CA22GENIChomozygous116489291
84969431249694313GA19GENIChomozygous116489293
84969434549694346AG17GENIChomozygous116489295
84969499249694993GC29GENIChomozygous116489297
84969566249695663TC35GENIChomozygous116489299
84969826649698267TC32GENIChomozygous116489301
84969867749698678AG27GENIChomozygous116489303
84969944249699443AG22GENIChomozygous116489305
84970027649700277TC32GENIChomozygous116489307
84970095549700956AG31GENIChomozygous116489309
84970230149702302CT19GENIChomozygous116489311
84970261249702613TC22GENIChomozygous116489313