chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3124898789124898790TC30GENIChomozygous111694964
3124902040124902041CT17GENIChomozygous112147908
3124902123124902124AT24GENIChomozygous112147909
3124903699124903700TC27GENIChomozygous111694972
3124903700124903701GA28GENIChomozygous112147911
3124904018124904019AG31GENIChomozygous111694975
3124909457124909458CT22GENIChomozygous111694983
3124911040124911041GT31GENIChomozygous112147921
3124911058124911059TA33GENIChomozygous111694986
3124902789124902790CT18GENICheterozygous120084959
3124913995124913996AG28GENIChomozygous120084961
3124917077124917078AT24GENIChomozygous112147927
3124920188124920189TC15GENIChomozygous112147929
3124921689124921690TC44GENIChomozygous111694998
3124922529124922530AG21GENIChomozygous111695000
3124925374124925375TC28GENIChomozygous111695003
3124925802124925803GA29GENIChomozygous111695005
3124927797124927798GT30GENIChomozygous112147937
3124927874124927875GA36GENIChomozygous112147939
3124928150124928151GA23GENIChomozygous111695008
3124928215124928216CT29GENIChomozygous112147941
3124928346124928347CT23GENIChomozygous120084963
3124928375124928376GT22GENICpossibly homozygous112147943
3124928382124928383AG23GENIChomozygous111695010
3124928568124928569GA33GENIChomozygous111695012
3124928577124928578TC31GENIChomozygous111695013
3124929115124929116CT18GENIChomozygous112147945
3124929374124929375GA25GENIChomozygous112147947
3124930276124930277GA25GENIChomozygous112147949
3124930434124930435CT22GENIChomozygous112147951
3124931318124931319GA24GENIChomozygous112147953
3124931329124931330TC26GENIChomozygous112147955
3124933527124933528TG23GENIChomozygous111695035