chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
98264872682648727TA47GENIChomozygous120456836
98264905782649058CT60GENIChomozygous120463448
98264982082649821GA55GENIChomozygous117588863
98265163582651636GA66GENIChomozygous117588873
98265002782650028G10GENIChomozygous135197256
98265006682650076AGAGGGAGAA3GENIChomozygous135197257
98265008982650090GA3GENIChomozygous135199833
98265408282654083CA41GENICpossibly homozygous120418796
98265479982654800GT61GENIChomozygous120456837
98265480682654807CA53GENIChomozygous120463449
98265666282656663CT58GENIChomozygous120456838
98265673582656736GA66GENIChomozygous117849638
98265683682656837AG66GENIChomozygous117588881
98265693582656936TC71GENIChomozygous117588883
98265840882658409AG57GENIChomozygous117588887
98265855982658560AG53GENIChomozygous120456839
98265862282658623AC54GENIChomozygous117849640
98265896282658963CA62GENIChomozygous117849641
98265974282659743AT65GENIChomozygous120456840
98266000182660002AG52GENIChomozygous117849643
98266003782660038TG52GENIChomozygous117849644
98266233782662338CT71GENIChomozygous120456841
98266287482662875CA58GENIChomozygous120456842
98266393182663932TG54GENIChomozygous120456843
98266517482665194ATCCACCCACCCACCCATCT15GENIChomozygous135197258
98265234382652345CC42GENIChomozygous131452312
98265722482657224A57GENICpossibly homozygous131452313
98266567882665678GTGA50GENIChomozygous131452315