chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5142136743142136744TC11GENIChomozygous631116904
5142136796142136797GA18GENICpossibly homozygous631116905
5142137497142137498A-19GENIChomozygous745549505
5142137565142137566GC10GENIChomozygous631116906
5142137568142137569GC11GENIChomozygous631116907
5142139858142139859GA14GENIChomozygous631116908
5142140081142140082GGGAGAAAATTCCAGTCAAGACACAATCTTTCTCAAAAGCTGTAACGAGGAGCAGGGAGGGCTGCTGA3GENICheterozygous745549506
5142140981142140982T-13GENIChomozygous745549507
5142141200142141201A-11GENIChomozygous745549508
5142141390142141391AAAACTCAATTACAAATGTCAACCAAATCCCTTCCAGCCGGTCTGTGATG3GENIChomozygous745549509
5142141528142141529CT23GENICpossibly homozygous631116909
5142142605142142606GGA2GENICheterozygous745549510
5142142874142142875TC26GENICpossibly homozygous631116910
5142143881142143882TTAAAA1GENIChomozygous745549513
5142144282142144283AAT3GENICheterozygous745549514
5142144334142144335CT14GENICheterozygous631116911
5142144913142144914CT22GENIChomozygous631116912
5142145195142145196GA13GENICpossibly homozygous631116913
5142146031142146032TC20GENICpossibly homozygous631116914
5142146401142146402CG13GENIChomozygous631116915
5142146554142146555GC33GENICpossibly homozygous631116916
5142147110142147111AG10GENICheterozygous631116917
5142147896142147897CCTAAG9GENIChomozygous745549517
5142148048142148049GT34GENICpossibly homozygous631116918
5142148411142148412AC25GENICpossibly homozygous631116919
5142148784142148785CCT12GENICpossibly homozygous745549518
5142148807142148808CT13GENIChomozygous631116920
5142148851142148852TG3GENIChomozygous631116921
5142149215142149216AC20GENICheterozygous631116922
5142149775142149776CG19GENIChomozygous631116923
5142150323142150324A-4GENIChomozygous745549519
5142150606142150607TTG4GENICheterozygous745549520
5142150612142150613AG7GENICheterozygous631116924
5142151431142151432GGT7GENIChomozygous745549521