chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101407832114078322TC56GENIChomozygous142218460
101407987514079876GA51GENIChomozygous142218461
101408156314081564CT56GENIChomozygous142218462
101408206614082067AG61GENIChomozygous142218463
101408215814082159AT66GENICpossibly homozygous142218464
101408235214082353TC56GENIChomozygous142218465
101408281814082831GGTTCGGTCCCCA47GENIChomozygous142196907
101408290414082908AACA50GENIChomozygous142196908
101408485414084855TG31GENIChomozygous142218466
101408508214085083G57GENIChomozygous142196909
101408596414085965CT55GENIChomozygous142218467
101408628514086286AG43GENIChomozygous142218468
101408793514087936CT57GENIChomozygous142218469
101408808914088090AG61GENIChomozygous142218470
101409083214090833AG63GENIChomozygous142218471
101409085614090857AC66GENICpossibly homozygous142218472
101409185214091857TGGTT29GENIChomozygous142196910
101409388114093882TG55GENIChomozygous142218473
101409435214094353AC57GENIChomozygous142218474
101409608514096113TGTGTGTATGTATGTATATATGTACGTA15GENIChomozygous145727770
101410052314100524CT50GENIChomozygous142218475
101410338014103382AA52GENIChomozygous142196911
101410365214103653TC65GENIChomozygous142218476
101410411214104113TC50GENIChomozygous142218477
101408403314084034TC47GENIChomozygous138725967
101410203114102032T21GENICheterozygous403276920
101410203114102032TC21GENICheterozygous403276921