chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
186136551261365513TC10GENIChomozygous633116566
186136559161365592GT8GENIChomozygous633116567
186136603761366038CG26GENIChomozygous633116568
186136605861366059TC26GENIChomozygous633116569
186136608961366090CG29GENIChomozygous633116570
186136621861366219TG28GENICpossibly homozygous633116571
186136628361366284GA27GENIChomozygous633116572
186136653661366537GA14GENIChomozygous633116573
186136655861366559GA14GENIChomozygous633116574
186136656961366570GT14GENIChomozygous633116575
186136658461366585GGGT9GENIChomozygous746629008
186136662861366641ATTGGGCAATGTC-------------5GENIChomozygous746629010
186136704661367047GA24GENIChomozygous633116576
186136720761367208AG11GENIChomozygous633116577
186136728861367289AAC9GENIChomozygous746629011
186136735161367352TA12GENIChomozygous633116578
186136737461367375GGTT12GENICheterozygous746629013
186136737461367375GGTTT12GENICpossibly homozygous746629014
186136746761367468AG14GENIChomozygous633116579
186136757061367571GT17GENIChomozygous633116580
186136828561368286GC21GENIChomozygous633116581
186136851561368516TC18GENIChomozygous633116582
186136857661368577TC19GENIChomozygous633116583
186136896561368966GC23GENIChomozygous633116584