chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
191147414411474145TC15GENIChomozygous109636727
191147913711479138CT17GENIChomozygous109636729
191148047411480475AG25GENIChomozygous109636731
191148094011480941AG26GENIChomozygous109636733
191148271411482715AC31GENIChomozygous109764847
191148313011483131CA23GENIChomozygous109636735
191148454311484544AG28GENIChomozygous109636737
191148521311485214CG13GENIChomozygous109636739
191148626311486264AG17GENIChomozygous109636741
191148629511486296CT15GENIChomozygous109636743
191148933111489332AG17GENIChomozygous109636745
191149045711490458GA17GENIChomozygous109636747
191149213611492137CT16GENIChomozygous109636749
191149290811492909GA23GENIChomozygous109636751
191149313211493133AG25GENIChomozygous109636753
191149431111494312GA28GENIChomozygous109636755
191149562611495627AT13GENIChomozygous109636761
191149653011496531CT25GENIChomozygous109636763
191149738311497384CT22GENIChomozygous109636765
191149792011497921TG24GENIChomozygous109636767
191150462111504622AT19GENIChomozygous109636779
191149867911498680AC18GENIChomozygous109636769
191149980011499801GT19GENIChomozygous109636771
191150140011501401AG12GENIChomozygous109636773
191150254811502549CA24GENIChomozygous109636775
191150437811504379GT23GENIChomozygous109636777
191150509911505100AG25GENIChomozygous109636781
191150563111505632GA24GENIChomozygous109636783
191150564911505650TC26GENIChomozygous109636785
191150568511505686CT26GENIChomozygous109636787
191150579011505791CT22GENIChomozygous109636789
191150591911505920TC21GENIChomozygous109636791
191150613911506140GA26GENIChomozygous109636793
191150620311506204AG29GENIChomozygous109636795
191150632611506327CT26GENIChomozygous109636797
191150659711506598GA29GENIChomozygous109636799
191150760211507603GA24GENIChomozygous109636801
191150760411507605CT23GENIChomozygous109636803