chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
186136551261365513TC17GENIChomozygous46483562
186136559161365592GT47GENIChomozygous46483563
186136603761366038CG25GENIChomozygous46483567
186136605861366059TC25GENIChomozygous46483568
186136608961366090CG26GENIChomozygous46483569
186136621861366219TG26GENIChomozygous46483570
186136628361366284GA30GENIChomozygous46483571
186136653661366537GA10GENIChomozygous46483572
186136655861366559GA10GENIChomozygous46483573
186136656961366570GT9GENIChomozygous46483574
186136658461366585GGGT7GENIChomozygous46483575
186136662861366641ATTGGGCAATGTC-------------9GENIChomozygous46483577
186136704661367047GA74GENICpossibly homozygous46483578
186136720761367208AG33GENIChomozygous46483579
186136728861367289AAC34GENIChomozygous46483580
186136735161367352TA19GENIChomozygous46483581
186136737461367375GGTTT13GENIChomozygous46483582
186136746761367468AG34GENIChomozygous46483583
186136757061367571GT22GENIChomozygous46483584
186136828561368286GC15GENIChomozygous46483585
186136851561368516TC10GENIChomozygous46483586
186136857661368577TC21GENIChomozygous46483587
186136896561368966GC24GENIChomozygous46483588