chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3124898789124898790TC20GENIChomozygous111694964
3124902040124902041CT18GENIChomozygous112147908
3124902123124902124AT9GENIChomozygous112147909
3124904018124904019AG19GENIChomozygous111694975
3124904143124904144GC33GENIChomozygous112147913
3124904541124904542TC14GENIChomozygous112147915
3124906117124906118CA13GENIChomozygous112147917
3124907565124907566AG17GENIChomozygous111694981
3124907571124907572CT21GENIChomozygous112147919
3124909457124909458CT8GENIChomozygous111694983
3124911058124911059TA16GENIChomozygous111694986
3124915745124915746GA23GENIChomozygous112147925
3124911040124911041GT11GENIChomozygous112147921
3124914346124914347CT22GENIChomozygous112147923
3124917077124917078AT15GENIChomozygous112147927
3124920188124920189TC17GENIChomozygous112147929
3124920997124920998GA13GENIChomozygous112147931
3124920998124920999CA13GENIChomozygous112147933
3124921689124921690TC23GENIChomozygous111694998
3124922529124922530AG14GENIChomozygous111695000
3124925374124925375TC14GENIChomozygous111695003
3124925802124925803GA21GENIChomozygous111695005
3124927423124927424CT30GENIChomozygous112147935
3124927797124927798GT21GENIChomozygous112147937
3124927874124927875GA16GENIChomozygous112147939
3124928150124928151GA19GENIChomozygous111695008
3124928215124928216CT22GENIChomozygous112147941
3124928375124928376GT11GENIChomozygous112147943
3124928382124928383AG9GENIChomozygous111695010
3124928568124928569GA15GENIChomozygous111695012
3124928577124928578TC10GENIChomozygous111695013
3124929115124929116CT17GENIChomozygous112147945
3124929374124929375GA27GENIChomozygous112147947
3124930276124930277GA23GENIChomozygous112147949
3124930434124930435CT6GENIChomozygous112147951
3124931318124931319GA18GENIChomozygous112147953
3124931329124931330TC16GENIChomozygous112147955
3124933527124933528TG21GENIChomozygous111695035
3124921750124921751CT7GENIChomozygous125894686
3124931714124931715GA4GENIChomozygous125835143