chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
171306407713064078GA5GENIChomozygous111169328
171306716713067168GA23GENIChomozygous119265428
171306727713067278TG9GENICheterozygous125532802
171306729313067294AG20GENIChomozygous119265435
171306739513067396GA22GENICheterozygous119265443
171306744513067446GA7GENICheterozygous119328672
171306745913067460TC5GENICheterozygous119356631
171306747913067480AG5GENIChomozygous125498576
171306621213066213AG27GENIChomozygous110962160
171306659913066600AG23GENIChomozygous110962163
171306675513066756GC12GENIChomozygous110962165
171306731813067319CT26GENIChomozygous125498574
171306742313067424AG27GENICpossibly homozygous125498575
171306748013067481AT5GENICheterozygous124302276
171306748013067481AT5GENICheterozygous124302276
171306748013067481AC3GENICheterozygous125532803
171306748013067481AC3GENICheterozygous125532803
171306748113067482AG7GENIChomozygous124302277
171306750713067508TC12GENICheterozygous119265445
171306753613067537TC22GENICheterozygous119265447
171306787613067877CT18GENIChomozygous110962167
171306787713067878AG18GENIChomozygous110962169
171306796213067963AG15GENIChomozygous110962171
171306837313068374TC18GENIChomozygous110962173
171306859213068593CG18GENICheterozygous110962177
171306863813068639AG17GENICpossibly homozygous110962179
171306905513069056CG20GENIChomozygous110962181
171306911713069118TC18GENIChomozygous110962183
171306921013069211GC17GENIChomozygous110962185
171306948213069483CT5GENIChomozygous110962187