chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5172988477172988478CT44GENIChomozygous114093938
5172988547172988548CT33GENIChomozygous114293063
5172989352172989353AT33GENIChomozygous114093940
5172989614172989615GA38GENIChomozygous114293065
5172991729172991730CT43GENIChomozygous114093944
5172992105172992106GA51GENIChomozygous114093946
5172992198172992199GA41GENIChomozygous114293067
5172992565172992566AG28GENIChomozygous114093948
5172993973172993974GT29GENIChomozygous114293069
5172995951172995952GT8GENIChomozygous114163363
5172996957172996958AT30GENIChomozygous114093960
5172998654172998655GC35GENIChomozygous114293071
5172998767172998768CT47GENIChomozygous114093962
5173001139173001140AG15GENIChomozygous114093964
5173002436173002437AG22GENICpossibly homozygous118859200
5173002437173002438CT22GENICpossibly homozygous118848140
5173003473173003474CT19GENIChomozygous114093968
5173005567173005568CG15GENIChomozygous114093970
5173007199173007200AG30GENIChomozygous114093972
5173008879173008880GA37GENIChomozygous114093974
5173010154173010155GA35GENIChomozygous114293073
5173010201173010202AT33GENIChomozygous114093976
5173014454173014455GA24GENIChomozygous114093978
5173015291173015292AG29GENIChomozygous114093980