chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
31375163713751638GC11GENIChomozygous111451867
31375486213754863TC15GENIChomozygous111451868
31375542613755427GA16GENIChomozygous111451869
31375630513756306GA20GENIChomozygous111451870
31375700213757003GA19GENIChomozygous111451871
31375717813757179CT26GENIChomozygous111451872
31375998913759990TC21GENIChomozygous111451873
31376042913760430GT22GENIChomozygous111451874
31376170913761710GA22GENIChomozygous111451875
31376592413765925AG25GENIChomozygous111451876
31376837613768377AT20GENIChomozygous111451877
31376868913768690TC13GENIChomozygous111451878
31376883113768832GA25GENIChomozygous111451879
31376900513769006GA25GENIChomozygous111451880
31377590613775907TA12GENIChomozygous111451881
31377622713776228CT24GENIChomozygous111451882
31377705713777058GA9GENIChomozygous111451883
31378069813780699TC22GENIChomozygous111451884
31378126113781262TC18GENIChomozygous111451885
31378299313782994GA17GENIChomozygous111451886
31378427913784280AG3GENICheterozygous125808400
31378497113784972AG21GENIChomozygous111451887
31378669513786696TC19GENIChomozygous111451888
31378895313788954AG4GENIChomozygous125808401
31379027813790279TG13GENIChomozygous111451891
31379151413791515TC19GENIChomozygous111451894
31379357413793575TC6GENICheterozygous125808402
31379357513793576CT7GENIChomozygous125808403
31379999913800000CT6GENIChomozygous111451897
31380150913801510CT14GENICheterozygous111451899
31380187413801875GA14GENIChomozygous111451900
31380350513803506CG17GENIChomozygous111451901
31380642513806426GA15GENIChomozygous111451902
31380803613808037AG21GENIChomozygous111451903
31380852413808525AC11GENIChomozygous111451904
31380913713809138AG21GENIChomozygous111451905
31381055413810555GA18GENIChomozygous111451906
31381152613811527TC18GENIChomozygous111451907
31381237113812372AG24GENIChomozygous111451908
31381349213813493GA26GENIChomozygous111451909
31381468413814685CT4GENIChomozygous111451910
31381534513815346AG22GENIChomozygous111451911
31381779213817793AG16GENIChomozygous111451912