chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7120717939120717940CT20GENICpossibly homozygous116081944
7120717980120717981AC16GENIChomozygous116081945
7120718002120718003AG21GENIChomozygous116081946
7120718603120718604TC30GENIChomozygous116081947
7120720857120720858GA28GENIChomozygous116081950
7120720954120720955GA34GENICpossibly homozygous116409513
7120720996120720997AG32GENIChomozygous116409514
7120721167120721168CT23GENIChomozygous116409515
7120721764120721765CT30GENIChomozygous116409517
7120725358120725359AT24GENIChomozygous118259119
7120725618120725619CG25GENIChomozygous116081952
7120726101120726102CT25GENIChomozygous115856964
7120732091120732092TA25GENIChomozygous115856970
7120733282120733283TC34GENIChomozygous115856974
7120733297120733298GA31GENIChomozygous116409522
7120734372120734373CT18GENIChomozygous116409523
7120739176120739177AC12GENIChomozygous115856978
7120741651120741652CT32GENIChomozygous116409524
7120741692120741693CT37GENIChomozygous116409525
7120741738120741739CT32GENIChomozygous115856984