chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141761819017618191AC33GENIChomozygous936192172
141761837217618373AC28GENIChomozygous936192173
141761868417618685TC34GENIChomozygous936192174
141761936417619365TC24GENIChomozygous936192175
141761941517619416CG7GENIChomozygous936192176
141761943517619436CT8GENIChomozygous936192177
141761944417619445TC12GENIChomozygous936192178
141761952317619524CT13GENIChomozygous936192179
141762012717620128GA33GENIChomozygous936192180
141762138217621383TC26GENIChomozygous936192181
141762151417621515CT18GENIChomozygous936192182
141762256517622566TA31GENIChomozygous936192183
141762270917622710CT23GENIChomozygous936192184
141762355617623557AG36GENIChomozygous936192185
141762428217624283TA22GENIChomozygous936192186
141762439017624391TC21GENIChomozygous936192187
141762512217625123CG17GENIChomozygous936192188
141762520417625205TA21GENIChomozygous936192189
141762529517625296GA40GENIChomozygous936192190
141762557417625575CT29GENIChomozygous936192191
141762588517625886AG25GENIChomozygous936192192
141762834817628349GC30GENIChomozygous936192193
141762864117628642CT21GENIChomozygous936192194
141762944817629449AG12GENIChomozygous936192195
141762984117629842TC28GENIChomozygous936192196
141763004517630046GA33GENIChomozygous936192197
141763060517630606TA21GENIChomozygous936192198
141763098317630984TC29GENIChomozygous936192199
141763113017631131GA28GENIChomozygous936192200
141763137017631371AG23GENIChomozygous936192201