chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
171306407713064078GA44GENIChomozygous111169328
171306621213066213AG47GENIChomozygous110962160
171306659913066600AG56GENICpossibly homozygous110962163
171306675513066756GC40GENIChomozygous110962165
171306716713067168GA57GENICpossibly homozygous119265428
171306723913067240AG89GENICheterozygous119265429
171306727713067278TA78GENICheterozygous119265432
171306728313067284CA85GENICheterozygous119265433
171306729313067294AG84GENICpossibly homozygous119265435
171306730413067305AG124GENICheterozygous119265436
171306731113067312GA124GENICheterozygous119265437
171306731313067314CA124GENICheterozygous119265438
171306732313067324AT146GENICheterozygous119265439
171306732813067329AG151GENICheterozygous119265440
171306736713067368AG155GENICheterozygous119265441
171306736913067370GA160GENICheterozygous119265442
171306739513067396GA148GENICheterozygous119265443
171306742313067424GA98GENICheterozygous119265444
171306745913067460TC57GENICheterozygous119356631
171306750713067508TC63GENICheterozygous119265445
171306753613067537TC56GENICpossibly homozygous119265447
171306787613067877CT57GENIChomozygous110962167
171306787713067878AG57GENIChomozygous110962169
171306796213067963AG57GENIChomozygous110962171
171306837313068374TC33GENIChomozygous110962173
171306859213068593CG31GENIChomozygous110962177
171306863813068639AG22GENIChomozygous110962179
171306905513069056CG58GENIChomozygous110962181
171306911713069118TC61GENIChomozygous110962183
171306921013069211GC51GENIChomozygous110962185
171306948213069483CT22GENIChomozygous110962187