chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3124897903124897904AC10GENIChomozygous111694962
3124898789124898790TC19GENIChomozygous111694964
3124903699124903700TC15GENIChomozygous111694972
3124903961124903962CT19GENIChomozygous111694973
3124904018124904019AG17GENIChomozygous111694975
3124904937124904938TC28GENIChomozygous111694978
3124905847124905848CT5GENIChomozygous111694980
3124907565124907566AG20GENIChomozygous111694981
3124909457124909458CT5GENIChomozygous111694983
3124909932124909933CT22GENIChomozygous111694985
3124911058124911059TA18GENIChomozygous111694986
3124912220124912221TG23GENIChomozygous111694988
3124916650124916651GA16GENIChomozygous111694991
3124917131124917132CT12GENIChomozygous111694993
3124918763124918764GA23GENIChomozygous111694995
3124919878124919879CG24GENIChomozygous111694996
3124921689124921690TC26GENIChomozygous111694998
3124922529124922530AG19GENIChomozygous111695000
3124925374124925375TC10GENIChomozygous111695003
3124925802124925803GA23GENIChomozygous111695005
3124928071124928072TC11GENIChomozygous111695006
3124928150124928151GA15GENIChomozygous111695008
3124928382124928383AG21GENIChomozygous111695010
3124928568124928569GA9GENIChomozygous111695012
3124928577124928578TC8GENIChomozygous111695013
3124929152124929153GC23GENIChomozygous111695015
3124929264124929265GT25GENIChomozygous111695017
3124930540124930541GA25GENIChomozygous111695020
3124931426124931427AG28GENIChomozygous111695023
3124931441124931442CT27GENIChomozygous111695025
3124932393124932394TG6GENIChomozygous111695030
3124932395124932396GA6GENIChomozygous111695032
3124933346124933347GA16GENIChomozygous111695033
3124933527124933528TG20GENIChomozygous111695035