chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
31375163713751638GC16GENIChomozygous111451867
31375486213754863TC20GENIChomozygous111451868
31375542613755427GA20GENIChomozygous111451869
31375630513756306GA36GENIChomozygous111451870
31375700213757003GA24GENIChomozygous111451871
31375717813757179CT28GENIChomozygous111451872
31375998913759990TC20GENIChomozygous111451873
31376042913760430GT9GENIChomozygous111451874
31376170913761710GA32GENIChomozygous111451875
31376592413765925AG30GENIChomozygous111451876
31376837613768377AT29GENIChomozygous111451877
31376868913768690TC36GENIChomozygous111451878
31376883113768832GA34GENIChomozygous111451879
31376900513769006GA26GENIChomozygous111451880
31377590613775907TA21GENIChomozygous111451881
31377622713776228CT19GENIChomozygous111451882
31377705713777058GA15GENIChomozygous111451883
31378069813780699TC30GENIChomozygous111451884
31378126113781262TC32GENIChomozygous111451885
31378299313782994GA38GENIChomozygous111451886
31378497113784972AG30GENIChomozygous111451887
31378669513786696TC36GENIChomozygous111451888
31379027813790279TG23GENIChomozygous111451891
31379139013791391TG37GENIChomozygous111451893
31379151413791515TC24GENIChomozygous111451894
31379718613797187CT22GENIChomozygous111451896
31379999913800000CT28GENIChomozygous111451897
31380187413801875GA32GENIChomozygous111451900
31380350513803506CG26GENICpossibly homozygous111451901
31380642513806426GA23GENIChomozygous111451902
31380803613808037AG33GENIChomozygous111451903
31380852413808525AC29GENIChomozygous111451904
31380913713809138AG13GENIChomozygous111451905
31381055413810555GA21GENIChomozygous111451906
31381152613811527TC31GENIChomozygous111451907
31381237113812372AG25GENIChomozygous111451908
31381349213813493GA22GENIChomozygous111451909
31381534513815346AG30GENIChomozygous111451911
31381779213817793AG32GENIChomozygous111451912