chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101407832114078322TC20GENIChomozygous142218460
101407987514079876GA27GENIChomozygous142218461
101408156314081564CT27GENIChomozygous142218462
101408206614082067AG24GENIChomozygous142218463
101408215814082159AT26GENIChomozygous142218464
101408235214082353TC19GENIChomozygous142218465
101408281814082831GGTTCGGTCCCCA14GENIChomozygous142196907
101408290414082908AACA22GENIChomozygous142196908
101408403314084034TC21GENIChomozygous138725967
101408485414084855TG20GENIChomozygous142218466
101408508214085083G21GENIChomozygous142196909
101408596414085965CT24GENIChomozygous142218467
101408628514086286AG24GENIChomozygous142218468
101408793514087936CT18GENIChomozygous142218469
101408808914088090AG22GENIChomozygous142218470
101409083214090833AG24GENIChomozygous142218471
101409085614090857AC26GENIChomozygous142218472
101409185214091857TGGTT20GENIChomozygous142196910
101409388114093882TG27GENIChomozygous142218473
101409435214094353AC26GENIChomozygous142218474
101410052314100524CT20GENIChomozygous142218475
101410338014103382AA18GENIChomozygous142196911
101410365214103653TC35GENIChomozygous142218476
101410411214104113TC23GENIChomozygous142218477