chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1234469123234469124AG18GENIChomozygous625989103
1234469351234469352AG25GENIChomozygous625989104
1234469398234469399CA23GENIChomozygous625989105
1234469417234469428GGTTAGGTATG-----------17GENIChomozygous742977872
1234469452234469453AT22GENIChomozygous625989106
1234469818234469819AG18GENIChomozygous625989107
1234469933234469934GC22GENIChomozygous625989108
1234470030234470031TG21GENIChomozygous625989109
1234470289234470290TA30GENIChomozygous625989110
1234470714234470715CT29GENIChomozygous625989111
1234470890234470897TTTTTTT-------15GENIChomozygous742977873
1234471020234471021CG19GENIChomozygous625989112
1234471256234471257A-21GENIChomozygous742977876
1234471270234471271TG27GENIChomozygous625989113
1234471924234471925TTAA25GENIChomozygous742977877
1234472005234472006TC16GENIChomozygous625989114
1234472079234472080CCTCT22GENIChomozygous742977878
1234472264234472265TTA16GENIChomozygous742977879
1234472293234472294AT19GENIChomozygous625989115
1234472294234472295AT19GENIChomozygous625989116
1234472407234472408TC15GENIChomozygous625989117
1234472917234472918CT31GENIChomozygous625989118
1234472971234472972TC32GENIChomozygous625989119
1234473171234473172GGT30GENIChomozygous742977881
1234473203234473204CT31GENIChomozygous625989120
1234473311234473312GT16GENIChomozygous625989121
1234473450234473451AC29GENIChomozygous625989122
1234473668234473669TTC32GENIChomozygous742977882
1234473718234473719AAT28GENIChomozygous742977883
1234473732234473733CT27GENIChomozygous625989123
1234473747234473748AG28GENIChomozygous625989124
1234473925234473926AG24GENIChomozygous625989125
1234474407234474408AC32GENIChomozygous625989126
1234474408234474409GA32GENIChomozygous625989127
1234474438234474439CA28GENIChomozygous625989128
1234475017234475018TC32GENIChomozygous625989129
1234475032234475033TC30GENIChomozygous625989130
1234475135234475136T-22GENIChomozygous742977884
1234475293234475294AC20GENIChomozygous625989131
1234476225234476226GGTT21GENIChomozygous742977886
1234476378234476382CCTT----24GENIChomozygous742977887
1234476652234476653AG20GENIChomozygous625989132
1234476862234476863AC14GENIChomozygous625989133
1234477039234477041AA--17GENIChomozygous742977888
1234477098234477099TC27GENIChomozygous625989134
1234477122234477123AG34GENIChomozygous625989135
1234477776234477777AAC30GENIChomozygous742977890
1234477909234477910CT27GENIChomozygous625989136
1234477957234477967AGTGTGTGTG----------8GENICpossibly homozygous742977895
1234478098234478099GC25GENIChomozygous625989137
1234478456234478457AG25GENIChomozygous625989138
1234478458234478459GA26GENIChomozygous625989139
1234478482234478483TC25GENIChomozygous625989140
1234478529234478535ACAGAC------25GENIChomozygous742977896
1234478778234478779GA24GENIChomozygous625989141
1234478837234478838AG28GENIChomozygous625989142
1234478861234478862CA25GENIChomozygous625989143
1234478886234478887AG23GENIChomozygous625989144
1234479033234479034GA24GENIChomozygous625989145
1234479404234479405GA19GENIChomozygous625989146
1234479509234479510A-6GENIChomozygous742977897
1234479563234479564CA7GENIChomozygous625989147
1234479881234479882C-25GENIChomozygous742977898
1234480412234480415TTT---15GENICheterozygous742977899
1234480413234480415TT--15GENICheterozygous742977900
1234480414234480415T-15GENICheterozygous742977901