chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
186136544961365450TG37GENICheterozygous505271225
186136551261365513TC30GENIChomozygous501681330
186136559161365592GT38GENIChomozygous501681331
186136577961365780CCCT9GENICheterozygous684897490
186136577961365780CCCCCT9GENICheterozygous684897491
186136577961365780CCCCT9GENICheterozygous684897492
186136603761366038CG54GENIChomozygous501681332
186136605861366059TC55GENIChomozygous501681333
186136608961366090CG56GENIChomozygous501681334
186136621861366219TG44GENIChomozygous501681335
186136628361366284GA35GENIChomozygous501681336
186136653661366537GA12GENICpossibly homozygous501681337
186136655861366559GA17GENIChomozygous505271226
186136656961366570GT18GENIChomozygous505271227
186136658461366585GGGT15GENICpossibly homozygous684897493
186136658461366585GGGTT15GENICheterozygous684897494
186136662861366641ATTGGGCAATGTC-------------9GENIChomozygous684897495
186136704661367047GA41GENIChomozygous501681338
186136720761367208AG40GENIChomozygous501681339
186136728861367289AAC27GENIChomozygous684897496
186136735161367352TA44GENIChomozygous501681340
186136737461367375GGTTT37GENIChomozygous684897497
186136746761367468AG52GENIChomozygous501681341
186136757061367571GT59GENIChomozygous501681342
186136828561368286GC43GENIChomozygous501681343
186136851561368516TC44GENIChomozygous501681344
186136857661368577TC46GENICpossibly homozygous501681345
186136896561368966GC29GENIChomozygous501681346