chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3124898789124898790TC22GENIChomozygous111694964
3124902040124902041CT7GENIChomozygous112147908
3124902123124902124AT9GENIChomozygous112147909
3124903699124903700TC17GENIChomozygous111694972
3124903700124903701GA17GENIChomozygous112147911
3124904018124904019AG24GENIChomozygous111694975
3124904143124904144GC30GENIChomozygous112147913
3124907565124907566AG26GENIChomozygous111694981
3124907571124907572CT29GENIChomozygous112147919
3124909457124909458CT17GENIChomozygous111694983
3124911040124911041GT29GENIChomozygous112147921
3124911058124911059TA21GENIChomozygous111694986
3124914346124914347CT25GENIChomozygous112147923
3124915745124915746GA24GENIChomozygous112147925
3124917077124917078AT17GENIChomozygous112147927
3124920188124920189TC24GENIChomozygous112147929
3124920997124920998GA23GENIChomozygous112147931
3124920998124920999CA23GENIChomozygous112147933
3124921689124921690TC22GENIChomozygous111694998
3124922529124922530AG20GENIChomozygous111695000
3124925374124925375TC28GENIChomozygous111695003
3124925802124925803GA30GENIChomozygous111695005
3124927423124927424CT29GENIChomozygous112147935
3124927797124927798GT20GENIChomozygous112147937
3124927874124927875GA32GENIChomozygous112147939
3124928150124928151GA33GENIChomozygous111695008
3124928215124928216CT27GENIChomozygous112147941
3124928375124928376GT36GENIChomozygous112147943
3124928382124928383AG35GENIChomozygous111695010
3124928577124928578TC32GENIChomozygous111695013
3124929115124929116CT35GENIChomozygous112147945
3124929374124929375GA28GENIChomozygous112147947
3124930276124930277GA30GENIChomozygous112147949
3124930434124930435CT29GENIChomozygous112147951
3124931318124931319GA39GENIChomozygous112147953
3124931329124931330TC37GENIChomozygous112147955
3124933527124933528TG31GENIChomozygous111695035