chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
148110570681105706GAGG17GENICpossibly homozygous131144898
148115916081159161A44GENICheterozygous134102267
148113458181134582GA59GENIChomozygous113603622
148113968981139689A15GENICheterozygous132183091
148117249681172496C52GENIChomozygous129177967
148117374381173744C26GENIChomozygous129177968
148117374881173748AC25GENIChomozygous129177969
148117375481173757GGT22GENIChomozygous129177970
148120486881204869AC40GENIChomozygous118703707
148117377281173772C25GENIChomozygous129177971
148117378081173780CA24GENIChomozygous129177972
148117378481173785A23GENIChomozygous129177973
148119219981192199T45GENIChomozygous129177974
148120523781205238CT38GENIChomozygous118765445
148120829681208297GT40GENICpossibly homozygous131151477
148120971481209715GC60GENICheterozygous129212791
148120966981209670GC64GENICheterozygous129212787
148120967681209677GT58GENICheterozygous129212788
148120970781209708AC59GENICheterozygous129212789
148120970881209709GA59GENICheterozygous129212790
148121001781210018GA46GENICheterozygous118703719
148121004781210048GA54GENICheterozygous129212793
148121007981210080GT55GENICheterozygous129212794
148121009181210092AG52GENICheterozygous129212795
148121012181210122AC55GENICheterozygous129212796
148121012881210129GA56GENICheterozygous129212797
148121013781210138GT56GENICheterozygous129212798
148121014081210141GA57GENICheterozygous129212799
148121016081210161GT60GENICheterozygous118703730
148121028981210290AC52GENICheterozygous123941267
148121029781210298CA49GENICheterozygous123941268
148121029981210300CG48GENICheterozygous123941269
148121030981210310CT49GENICheterozygous123941270
148121031281210313CT48GENICheterozygous123941271
148121032081210321GC50GENICheterozygous123941272
148121032181210322GA51GENICheterozygous123941273
148121032581210326GA51GENICheterozygous123941274
148124222081242222AC53GENIChomozygous131144899
148121057281210573CT29GENIChomozygous113501556
148123237681232377AG59GENIChomozygous113501558