chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7120717939120717940CT26GENIChomozygous116081944
7120717980120717981AC22GENIChomozygous116081945
7120718002120718003AG27GENIChomozygous116081946
7120718603120718604TC36GENIChomozygous116081947
7120720857120720858GA40GENIChomozygous116081950
7120720954120720955GA29GENIChomozygous116409513
7120720996120720997AG27GENIChomozygous116409514
7120721167120721168CT21GENIChomozygous116409515
7120721371120721372TA10GENIChomozygous116409516
7120721764120721765CT20GENIChomozygous116409517
7120725358120725359AT27GENIChomozygous118259119
7120725618120725619CG32GENIChomozygous116081952
7120732091120732092TA18GENIChomozygous115856970
7120726101120726102CT33GENIChomozygous115856964
7120733282120733283TC34GENIChomozygous115856974
7120733297120733298GA35GENIChomozygous116409522
7120734372120734373CT19GENIChomozygous116409523
7120739176120739177AC9GENIChomozygous115856978
7120741651120741652CT24GENIChomozygous116409524
7120741692120741693CT22GENIChomozygous116409525
7120741738120741739CT23GENIChomozygous115856984