chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1170383693170383694CG18INTERGENICpossibly homozygous60940682
1170383953170383954AAGACT11INTERGENIChomozygous60940683
1170384180170384181CA8INTERGENIChomozygous60940684
1170384360170384361GA3GENICheterozygous61908990
1170384559170384560TC10GENIChomozygous60940685
1170384771170384772CT10GENICpossibly homozygous61908991
1170385213170385218CCTCC-----9GENIChomozygous60940686
1170385374170385375AT11GENIChomozygous61908992
1170386312170386313AAG16GENICpossibly homozygous61908994
1170386698170386699GA24GENIChomozygous60940690
1170386741170386742CT17GENIChomozygous60940691
1170387424170387425GC18GENICpossibly homozygous61908995