chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1170383693170383694CG12INTERGENIChomozygous60940682
1170383953170383954AAGACT2INTERGENIChomozygous60940683
1170384180170384181CA7INTERGENIChomozygous60940684
1170384360170384361GA1GENIChomozygous61908990
1170384559170384560TC11GENIChomozygous60940685
1170384771170384772CT12GENICpossibly homozygous61908991
1170385213170385218CCTCC-----6GENICheterozygous60940686
1170385374170385375AT13GENIChomozygous61908992
1170386312170386313AAG14GENIChomozygous61908994
1170386698170386699GA19GENIChomozygous60940690
1170386741170386742CT16GENIChomozygous60940691
1170387424170387425GC8GENIChomozygous61908995