chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1173382079173382080G-29GENIChomozygous60947547
1173383699173383700GA27GENIChomozygous60947548
1173385367173385368GGAA14GENICheterozygous60947549
1173385367173385368GGAAA14GENICheterozygous60947550
1173385367173385368GGAAAA14GENICheterozygous62174837
1173385915173385916CT17GENIChomozygous60947552
1173386712173386714GG--11GENIChomozygous60947553
1173387165173387166GGA25GENIChomozygous60947554
1173387215173387216AG25GENIChomozygous60947555
1173387579173387580GA31GENIChomozygous60947556
1173387762173387763CT17GENIChomozygous60947557
1173388254173388255GA19GENIChomozygous60947559
1173388311173388327AAAAAACAACAACAAC----------------7GENICpossibly homozygous60947562
1173388376173388377AAGAATGAATGAAT18GENIChomozygous60947565
1173388457173388458AG22GENIChomozygous60947566
1173388656173388657CCT31GENICpossibly homozygous60947567
1173389172173389173CT28GENIChomozygous60947568
1173389216173389217TC25GENIChomozygous60947569
1173389232173389233GA20GENIChomozygous60947570
1173389662173389663TC27GENIChomozygous60947571
1173389783173389784TA12GENIChomozygous60947572
1173389871173389872GA19GENIChomozygous60947573
1173390048173390049CG18GENIChomozygous60947574
1173390090173390091CT16GENIChomozygous60947575
1173390202173390203TC18GENIChomozygous60947576
1173390388173390389CCTGTG16GENICpossibly homozygous60947577
1173390388173390389CCTGTGTGTGTG16GENICheterozygous60947578
1173390403173390404CT22GENICpossibly homozygous60947579
1173390856173390857GA14GENIChomozygous60947580
1173391329173391330CA25GENIChomozygous60947581