chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
86076006960760070G51GENIChomozygous128596397
86076050160760502AG58GENIChomozygous116515857
86076093160760932TC52GENIChomozygous116515859
86076283260762833AG52GENIChomozygous116515861
86076455760764558AG69GENIChomozygous116515863
86076581060765811CT54GENIChomozygous116515865
86076868360768684AG49GENIChomozygous116515867
86076943860769439CT47GENIChomozygous116515869
86077137060771371AG55GENIChomozygous116515871
86077153060771531TC52GENIChomozygous116515873
86077212760772128GA54GENIChomozygous116515875
86076244060762440TTAAATGAA25GENICheterozygous132482705
86077573860775738AGC47GENIChomozygous128596398
86078573560785736GA33GENIChomozygous116515885
86078580360785804C38GENIChomozygous128596410
86078709660787097GA50GENIChomozygous116515887
86079409560794096TC51GENIChomozygous116515889
86079477060794771TC54GENIChomozygous116515891
86079509360795094GA52GENIChomozygous116515893
86079529360795294CA55GENIChomozygous116515895
86079772960797730CT45GENIChomozygous116515897
86079833660798337AG14GENIChomozygous117108845
86077791660777920TTTT40GENIChomozygous132122650