chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5131338331131338332CCTT22GENICpossibly homozygous55722148
5131340063131340064AC31GENIChomozygous55722151
5131341244131341245AG24GENIChomozygous55722153
5131341822131341823CG26GENICheterozygous55722157
5131342735131342736TC23GENIChomozygous55722160
5131343061131343062TC23GENIChomozygous55722162
5131343235131343236CT26GENIChomozygous55722165
5131345141131345142TC22GENIChomozygous55722167
5131345215131345216AG25GENIChomozygous55722170
5131345532131345533C-20GENIChomozygous55722172
5131345769131345770AC24GENIChomozygous55722174