chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103851292238512923AG27GENIChomozygous116565369
103851374038513741GA25GENIChomozygous116761897
103851432438514325GA32GENIChomozygous116761899
103851443538514436GA30GENIChomozygous116761901
103851472438514725GA26GENIChomozygous116761903
103851492438514925AG18GENIChomozygous116761905
103851528938515290AG16GENIChomozygous116761909
103851606038516061TC18GENIChomozygous116761911
103851716738517168GT21GENIChomozygous116761913
103852047838520479CT30GENIChomozygous116761915
103852227338522274AG24GENICpossibly homozygous116761917
103852430438524305TC23GENIChomozygous116761919
103852473838524739AT22GENIChomozygous116761921
103852478838524789CT22GENIChomozygous116761923
103852486238524863AG26GENIChomozygous116761925
103852584138525842AG26GENIChomozygous116761927
103852718738527188TA31GENIChomozygous116761929
103852750338527504AG18GENICpossibly homozygous116761931
103853010538530106GA16GENIChomozygous116761933
103853806338538064GA24GENIChomozygous116761935