chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
176162966361629664CT27GENICpossibly homozygous140156960
176162983861629839GT31GENIChomozygous140156961
176162986061629861CA30GENIChomozygous140156962
176163008961630093ACAC34GENIChomozygous140031524
176163009561630105GGAAAGAAAC34GENIChomozygous140031525
176163027661630277TA25GENIChomozygous140156963
176163072361630724TC28GENIChomozygous140156964
176163093361630933A28GENIChomozygous140031526
176163112461631130ATATAC12GENIChomozygous140031527
176163193661631936GTACCTGGTGCCCTG18GENIChomozygous140031528
176163254261632542GCC23GENIChomozygous140031529
176163254461632544A22GENIChomozygous140031530
176163274661632755TAGCCTGTC9GENIChomozygous140031531
176163275861632759CG10GENIChomozygous140156965
176163313361633133A15GENIChomozygous140031532
176163368661633687GA18GENIChomozygous140156966
176163509661635097AG15GENIChomozygous140156967
176163515561635155T9GENICpossibly homozygous140031533
176163541161635412CT11GENIChomozygous140156968
176163541461635415TC11GENIChomozygous140156969
176163583161635832AG9GENIChomozygous140156970
176163699861636999GC10GENIChomozygous140156971
176163700561637006AG9GENIChomozygous140156972