chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4169585402169585403TC78GENICheterozygous112946624
4169585483169585484CT66GENICheterozygous113313972
4169617380169617381TC40GENICheterozygous113215012
4169632050169632051CG29GENICheterozygous112946628
4169764081169764082GT5GENIChomozygous113067732
4169799917169799918AC32GENIChomozygous113313973
4169799963169799964CT32GENIChomozygous113313974
4169804815169804816GA41GENIChomozygous113313975
4169807539169807540TG21GENIChomozygous113313976
4169807578169807579GA34GENICheterozygous112946634
4169808853169808854AG26GENIChomozygous113313977
4169809047169809048TC39GENIChomozygous113313978
4169810658169810659GC41GENIChomozygous113313979
4169811111169811112CT34GENIChomozygous113313980
4169822901169822902GT10GENIChomozygous112946646
4169823053169823054GT10GENIChomozygous112946648
4169823067169823068CA5GENIChomozygous112946650
4169823071169823072TG5GENICheterozygous112946652
4169824430169824431AC37GENIChomozygous112946654
4169824481169824482TG37GENIChomozygous112946656
4169824667169824668CA26GENIChomozygous112946658
4169845279169845280GT16GENICpossibly homozygous113067734
4169845299169845300AT25GENIChomozygous112946690
4169845373169845374CA42GENIChomozygous112946692
4169845397169845398GT52GENIChomozygous112946694
4169881888169881889AG11GENIChomozygous112946941
4169882056169882057TG21GENIChomozygous113313981
4169893886169893887CA39GENIChomozygous112947012
4169905446169905447GA34GENICheterozygous112947068
4169905450169905451GA33GENICheterozygous113248414