chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
138046104180461042GA10GENIChomozygous114690444
138046574480465745TC8GENIChomozygous114405658
138046147080461472AA17GENIChomozygous131504773
138046207980462080CG12GENIChomozygous114566815
138046526380465264CT25GENIChomozygous114566816
138046599180465992GA17GENIChomozygous114566817
138046239980462400T7GENICheterozygous129078117
138046675080466751AG16GENIChomozygous114405662
138046927480469274T13GENIChomozygous131504774
138046963680469637TC6GENIChomozygous114405668
138046963980469640CT7GENIChomozygous114405670
138047002780470027T13GENIChomozygous129078119
138047017580470176CT25GENIChomozygous114405674
138047045580470456CT11GENIChomozygous114566818
138047141780471418TC16GENIChomozygous114405676
138047413980474139TG10GENIChomozygous129078121
138047464980474649A9GENIChomozygous131504775
138047835580478356TC16GENIChomozygous114566819
138047288880472889CT19GENIChomozygous114405677
138047436380474364GC19GENIChomozygous114405679
138047468880474689CT8GENIChomozygous114405681
138047486580474865A17GENICpossibly homozygous129078122
138047934180479341T16GENICheterozygous131504776