chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
27213830972138310G-25GENIChomozygous58883113
27213898672138987AG21GENIChomozygous58883115
27213912072139121TC21GENIChomozygous58883116
27213932972139330AG26GENIChomozygous58883117
27213938172139382TTTGTGTGTGTG8GENIChomozygous60484302
27213950372139504TTC11GENIChomozygous58883118
27213952972139536AGAGCAT-------2GENIChomozygous60484303
27213970172139702GT16GENIChomozygous58883119
27213992772139928TC34GENIChomozygous58883120
27214001672140017TC30GENIChomozygous58883121
27214011772140118A-19GENIChomozygous58883122
27214069472140695TTTTC2GENIChomozygous60484304
27214102672141027TC22GENIChomozygous58883123
27214222172142222GGCACA9GENICpossibly homozygous58883124
27214299172142992CT22GENIChomozygous59723795
27214053372140534AG19GENIChomozygous59723792
27214222172142222GGCACACACACA9GENICheterozygous60751352
27214371372143714CT9GENIChomozygous58883125
27214430272144303AT11GENIChomozygous58883126
27214438272144383GA20GENIChomozygous59723796
27214453972144540GGA6GENIChomozygous58883127
27214485272144853GA17GENIChomozygous58883128
27214528272145283T-21GENIChomozygous58883129
27214784272147843CT13GENIChomozygous58883130
27214796772147968GGT13GENICheterozygous58883131
27214796772147968GGTT13GENICpossibly homozygous59723797
27214838872148389AG17GENIChomozygous58883133