chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8117183108117183109TC26GENIChomozygous116671090
8117183890117183891TC25GENIChomozygous116671092
8117184516117184517GC21GENIChomozygous116671094
8117185898117185899CG14GENIChomozygous116671096
8117186602117186603TC24GENIChomozygous116671098
8117187259117187260TC22GENIChomozygous116671100
8117187620117187621TC24GENIChomozygous116671102
8117187986117187987AG24GENIChomozygous116671104
8117189553117189554GA24GENICpossibly homozygous116671106
8117190611117190612GA26GENIChomozygous116671108
8117190861117190862AG28GENIChomozygous116671110
8117193803117193804GT18GENIChomozygous116671114
8117194819117194820CT22GENIChomozygous116671116
8117197805117197806CA24GENIChomozygous116671118
8117201541117201542GA22GENIChomozygous116671122
8117209520117209521GA17GENIChomozygous116671128
8117209894117209895AG22GENIChomozygous116671132
8117209900117209901GA24GENIChomozygous116671134
8117209919117209920CT23GENIChomozygous116671136
8117210100117210101CG16GENIChomozygous116671138
8117210104117210105GA16GENIChomozygous116671140
8117210709117210710TC16GENIChomozygous116671144
8117210980117210981CT24GENIChomozygous116671146
8117212612117212613GA29GENIChomozygous116671148
8117212839117212840AG16GENIChomozygous116671150