chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1170383693170383694CG26INTERGENIChomozygous60940682
1170383953170383954AAGACT19INTERGENIChomozygous60940683
1170384180170384181CA32INTERGENIChomozygous60940684
1170384360170384361GA31GENIChomozygous61908990
1170384559170384560TC29GENIChomozygous60940685
1170384771170384772CT32GENIChomozygous61908991
1170385213170385218CCTCC-----13GENIChomozygous60940686
1170385374170385375AT29GENIChomozygous61908992
1170385289170385291AA--11GENICheterozygous62173148
1170385292170385293TTGTGTGTG11GENICheterozygous62173150
1170385294170385295C-11GENICheterozygous62173152
1170385298170385299A-13GENICheterozygous62173154
1170386312170386313AAG28GENIChomozygous61908994
1170386698170386699GA30GENIChomozygous60940690
1170386741170386742CT27GENIChomozygous60940691
1170387424170387425GC23GENICpossibly homozygous61908995