chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
513243481324349T-22GENIChomozygous56112106
513251641325165AG19GENIChomozygous56112108
513260691326081AAGGAAGGAAGG------------8GENIChomozygous56390031
513261481326152GAAG----29GENIChomozygous56112112
513275741327575TA30GENIChomozygous56112114
513276001327601TC29GENIChomozygous56112116
513284461328447AT25GENIChomozygous56112118
513293321329333TTC15GENICpossibly homozygous56112120
513296761329677AC32GENIChomozygous56112122
513303541330355CA37GENIChomozygous56112124
513305591330560CT30GENIChomozygous56112126
513317851331786GA18GENIChomozygous56112128
513329491332950AATGTGTCTTTGTT6GENICheterozygous56390034
513357451335746CT27GENIChomozygous56112132
513360711336072CT29GENIChomozygous56112134
513362781336279CT24GENIChomozygous56112136
513372971337298AC20GENIChomozygous56112138
513382751338276GGA32GENIChomozygous56112140
513393921339393AT21GENIChomozygous56112141
513394491339450CT19GENIChomozygous56112144
513404761340477AG29GENIChomozygous55182964
513406721340673CT20GENIChomozygous56112146
513409741340975GA28GENIChomozygous56112147
513413081341309GA20GENIChomozygous56112150
513415721341573CA24GENIChomozygous56112152