chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7129678202129678203GA38GENIChomozygous115887938
7129680775129680776CT38GENIChomozygous115887940
7129681328129681329TG2GENIChomozygous115887942
7129682792129682793CT29GENIChomozygous115887944
7129683228129683229AG43GENIChomozygous115887946
7129687228129687229CT29GENIChomozygous115887948
7129687601129687602AC27GENIChomozygous115887950
7129688708129688709TC38GENIChomozygous115887952
7129689311129689312AC5GENIChomozygous116084177
7129689313129689314TG2GENIChomozygous116084178
7129689568129689569TG10GENICpossibly homozygous115887954
7129691619129691620CA28GENIChomozygous115887956
7129696107129696108AG39GENIChomozygous115887958
7129696176129696177AG19GENIChomozygous115887960
7129697233129697234GT24GENIChomozygous115887962
7129697821129697822AG46GENIChomozygous115887964
7129699709129699710CT41GENIChomozygous115887966
7129699897129699898GA37GENIChomozygous115887968
7129700615129700616GA25GENIChomozygous115887970
7129700624129700625GA22GENIChomozygous115887972
7129700641129700642CT20GENIChomozygous115887974
7129700662129700663CT25GENIChomozygous115887976
7129700743129700744GA33GENIChomozygous115887978
7129700755129700756CG26GENIChomozygous115887981
7129700757129700758CT26GENIChomozygous115887983
7129700929129700930CG43GENIChomozygous115887985
7129701023129701024CA29GENIChomozygous115887987
7129701941129701942GA37GENIChomozygous115887989
7129702227129702228AG45GENIChomozygous115887991
7129705148129705149TC30GENIChomozygous115887993
7129711672129711673TC34GENIChomozygous115887995
7129718728129718729AG26GENIChomozygous115887997
7129721560129721561CT16GENIChomozygous115887999
7129721577129721578AG32GENIChomozygous115888001
7129721622129721623TG25GENIChomozygous115888003
7129721791129721792CG32GENIChomozygous115888005
7129687276129687277AG25GENICheterozygous116345565