chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5151559808151559811AGT---19GENIChomozygous56900191
5151560737151560738GA21GENIChomozygous56900193
5151560864151560865GA32GENIChomozygous56900195
5151561199151561200AG32GENIChomozygous55796989
5151563294151563295TG21GENIChomozygous55796990
5151563569151563570TG16GENIChomozygous55796992
5151563943151563944AC44GENIChomozygous56900197
5151564282151564283CCTTTT9GENIChomozygous56460874
5151565128151565129CT26GENIChomozygous56900199
5151565399151565400TTC26GENIChomozygous55796999
5151565449151565450CG44GENIChomozygous56900201
5151565509151565510CT40GENIChomozygous55797000
5151565633151565634CG35GENIChomozygous56900203
5151565656151565657TC31GENIChomozygous55797001
5151565708151565710TA--29GENIChomozygous55925219
5151565747151565748C-31GENIChomozygous55925221
5151565982151565983AG17GENIChomozygous55797004
5151566082151566083TA17GENIChomozygous55797005
5151567038151567042CTTC----12GENICheterozygous55797010
5151567108151567109AG11GENIChomozygous56900205
5151567392151567395TGC---13GENIChomozygous56710624
5151567467151567468CT14GENIChomozygous56900207
5151567541151567542AG15GENIChomozygous56189942
5151567931151567932G-32GENIChomozygous55797012
5151568128151568129AG23GENIChomozygous55797013
5151568463151568464AAT8GENIChomozygous55797014
5151568469151568470A-5GENIChomozygous55797015
5151568558151568559C-10GENIChomozygous55797017
5151569110151569111TC11GENIChomozygous55797019
5151569399151569400TC25GENIChomozygous55797021
5151570462151570464AA--4GENICheterozygous55797025
5151572164151572179AAAAAGGCCCCAAAA---------------1GENIChomozygous56532759
5151572330151572331GA6GENIChomozygous55797041
5151572348151572349AG2GENICheterozygous56900209
5151573939151573940CT16GENIChomozygous56900211