chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1239397559239397560AG26GENIChomozygous108586013
1239397738239397739AG26GENIChomozygous108586014
1239397759239397760TG29GENIChomozygous108586015
1239398195239398196CT46GENIChomozygous109205985
1239398237239398238GA48GENICpossibly homozygous108586017
1239398240239398241GC47GENIChomozygous108586018
1239398590239398591GT23GENIChomozygous109205987
1239401415239401416CT32GENIChomozygous109205989
1239401432239401433TG31GENICpossibly homozygous109205991
1239402220239402221TC41GENICpossibly homozygous108586030
1239403720239403721TC32GENIChomozygous109205993