chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1173382079173382080G-15GENIChomozygous714940967
1173383699173383700GA24GENIChomozygous576270769
1173385367173385368GGAA12GENICheterozygous714940968
1173385367173385368GGAAA12GENICheterozygous714940969
1173385367173385368GGAAAA12GENICheterozygous714940970
1173385915173385916CT9GENIChomozygous576270770
1173386712173386714GG--30GENIChomozygous714940971
1173387165173387166GGA21GENIChomozygous714940972
1173387215173387216AG11GENIChomozygous576270771
1173387579173387580GA8GENIChomozygous576270772
1173387762173387763CT7GENIChomozygous576270773
1173388254173388255GA10GENIChomozygous576270774
1173388311173388327AAAAAACAACAACAAC----------------4GENICheterozygous714940973
1173388376173388377AAGAATGAATGAAT16GENICheterozygous714940974
1173388376173388377AAGAATGAATGAATGAAT16GENICheterozygous714940975
1173388457173388458AG19GENIChomozygous576270775
1173388656173388657CCT14GENICpossibly homozygous714940977
1173389172173389173CT26GENIChomozygous576270776
1173389216173389217TC29GENIChomozygous576270777
1173389232173389233GA29GENIChomozygous576270778
1173389662173389663TC16GENIChomozygous576270779
1173389783173389784TA16GENIChomozygous576270780
1173389871173389872GA22GENIChomozygous576270781
1173390048173390049CG15GENIChomozygous576270782
1173390090173390091CT18GENIChomozygous576270783
1173390202173390203TC23GENIChomozygous576270784
1173390388173390389CCTGTG16GENIChomozygous714940978
1173390403173390404CT22GENIChomozygous576270785
1173390856173390857GA16GENIChomozygous576270786
1173391329173391330CA15GENIChomozygous576270787