chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5146534082146534094GGGTAGAGAGGA22GENIChomozygous143187270
5146536013146536013T26GENIChomozygous143187272
5146536014146536015AG26GENIChomozygous143260295
5146537467146537468AG16GENIChomozygous143260296
5146537534146537535AG21GENIChomozygous143260297
5146537615146537616T22GENICpossibly homozygous143187273
5146538286146538287TC16GENIChomozygous143260298
5146539188146539188G20GENIChomozygous143187274
5146539659146539660CT27GENIChomozygous143260299
5146540663146540664AG16GENIChomozygous143260300
5146541487146541488A19GENIChomozygous143187275
5146542095146542099ATAC20GENIChomozygous137347743
5146542990146542990G16GENIChomozygous143187276
5146543750146543751TC30GENIChomozygous143260301
5146543878146543879AG17GENIChomozygous143260302
5146544694146544702TTTGTTTG10GENIChomozygous143187277
5146546949146546950CT20GENIChomozygous143260303
5146547174146547175TC22GENIChomozygous143260304
5146544975146544976AT7GENIChomozygous154253301