chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
513243481324349T-22GENIChomozygous56112106
513251641325165AG21GENIChomozygous56112108
513260691326081AAGGAAGGAAGG------------12GENIChomozygous56390031
513261481326152GAAG----22GENIChomozygous56112112
513275741327575TA14GENIChomozygous56112114
513276001327601TC14GENIChomozygous56112116
513284461328447AT23GENIChomozygous56112118
513293321329333TTC16GENIChomozygous56112120
513296761329677AC21GENICpossibly homozygous56112122
513303541330355CA29GENIChomozygous56112124
513305591330560CT15GENIChomozygous56112126
513317851331786GA22GENIChomozygous56112128
513329491332950AATGTGTCTTTGTT3GENICheterozygous56390034
513357451335746CT18GENIChomozygous56112132
513360711336072CT31GENIChomozygous56112134
513362781336279CT34GENIChomozygous56112136
513372971337298AC21GENIChomozygous56112138
513382751338276GGA18GENICpossibly homozygous56112140
513393921339393AT18GENIChomozygous56112141
513394491339450CT16GENIChomozygous56112144
513404761340477AG25GENIChomozygous55182964
513406721340673CT22GENIChomozygous56112146
513409741340975GA27GENIChomozygous56112147
513413081341309GA34GENIChomozygous56112150
513415721341573CA28GENIChomozygous56112152