chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
174551599945516007CGATCTCC--------6GENICheterozygous47118868
174551653645516537CT18GENICpossibly homozygous47118869
174551669745516698TTAGAC11GENIChomozygous47118870
174551848345518484TTG19GENICpossibly homozygous47118873
174551980245519803GC22GENIChomozygous47118874
174552026145520262GA9GENICpossibly homozygous47118875
174552110145521102TC22GENIChomozygous47118885
174552267045522671GA8GENICpossibly homozygous47118886
174552315345523154TTC17GENIChomozygous47118887