chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
174023021540230215C18GENICpossibly homozygous140022404
174023034140230342TG38GENIChomozygous140114950
174023258740232588TC34GENIChomozygous140114951
174023354440233545TC29GENIChomozygous140114952
174023423140234232AT26GENIChomozygous140114953
174023433840234339AG29GENIChomozygous140114954
174023488840234889CG34GENIChomozygous140114955
174023552840235528AAAC15GENIChomozygous140022405
174023669940236700CA27GENICpossibly homozygous140114956
174023676340236764TC25GENIChomozygous140114957
174023695340236954TC27GENIChomozygous140114958
174023791440237915A22GENIChomozygous140022406
174023793540237936AG28GENIChomozygous140114959
174023844440238445C13GENIChomozygous140022407
174023908540239086AG23GENIChomozygous140114960
174023964140239642GC24GENIChomozygous140114961