chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2188745904188745905CT49GENIChomozygous110993892
2188746796188746797TC37GENIChomozygous110804688
2188747628188747629CT37GENIChomozygous110804689
2188748716188748717GC39GENICpossibly homozygous110804692
2188749427188749428CT41GENIChomozygous110169788
2188749939188749940AG41GENIChomozygous110804693
2188750224188750225GA37GENIChomozygous110804694
2188750226188750227TC37GENIChomozygous110169794
2188750903188750904GA52GENIChomozygous110993894
2188751316188751317TC30GENIChomozygous110804695
2188751685188751686TG41GENIChomozygous110169797
2188752166188752167TG45GENIChomozygous110169799
2188752438188752439AG60GENIChomozygous110169803
2188753603188753604GA41GENIChomozygous110993896
2188753994188753995CT37GENIChomozygous110993898
2188754271188754272AG30GENIChomozygous110169807
2188754333188754334AG33GENIChomozygous110169809
2188754860188754861CT36GENICheterozygous110993900
2188754921188754922TC24GENIChomozygous110169811
2188754949188754950AG25GENIChomozygous110169815
2188755052188755053CT38GENICpossibly homozygous110993902