chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5131338331131338332CCTT18GENICpossibly homozygous55722148
5131340063131340064AC15GENIChomozygous55722151
5131341244131341245AG30GENIChomozygous55722153
5131342735131342736TC30GENIChomozygous55722160
5131343061131343062TC23GENIChomozygous55722162
5131343235131343236CT24GENIChomozygous55722165
5131345141131345142TC20GENIChomozygous55722167
5131345215131345216AG29GENIChomozygous55722170
5131345532131345533C-15GENIChomozygous55722172
5131345769131345770AC20GENIChomozygous55722174