chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
186136551261365513TC3GENIChomozygous46483562
186136559161365592GT8GENIChomozygous46483563
186136603761366038CG10GENIChomozygous46483567
186136605861366059TC6GENIChomozygous46483568
186136608961366090CG9GENICpossibly homozygous46483569
186136621861366219TG14GENIChomozygous46483570
186136628361366284GA10GENIChomozygous46483571
186136653661366537GA8GENIChomozygous46483572
186136655861366559GA4GENIChomozygous46483573
186136656961366570GT1GENIChomozygous46483574
186136658461366585GGGT2GENIChomozygous46483575
186136662861366641ATTGGGCAATGTC-------------1GENIChomozygous46483577
186136704661367047GA6GENICheterozygous46483578
186136720761367208AG5GENICheterozygous46483579
186136728861367289AAC7GENICpossibly homozygous46483580
186136735161367352TA2GENIChomozygous46483581
186136737461367375GGTTT2GENIChomozygous46483582
186136746761367468AG11GENIChomozygous46483583
186136757061367571GT9GENIChomozygous46483584
186136828561368286GC12GENICheterozygous46483585
186136851561368516TC11GENIChomozygous46483586
186136857661368577TC11GENIChomozygous46483587
186136896561368966GC9GENICpossibly homozygous46483588