chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1240909893240909894TG4GENIChomozygous109540634
1240910286240910287CT17GENIChomozygous109540635
1240910304240910305GA16GENIChomozygous109540636
1240911972240911973TC12GENIChomozygous109540637
1240913993240913994AG21GENIChomozygous109540639
1240914672240914673TC20GENIChomozygous109540640
1240914673240914674GA20GENIChomozygous109540641
1240914891240914892GT11GENIChomozygous109540642
1240916187240916188TC14GENIChomozygous109540643
1240916222240916223TC20GENIChomozygous109540644
1240917229240917230CT27GENIChomozygous109540645
1240919547240919548TC16GENIChomozygous109540646
1240921982240921983CT13GENIChomozygous109540650
1240922514240922515CA28GENIChomozygous109540651
1240922777240922778GC10GENIChomozygous109540652
1240922794240922795GA10GENIChomozygous109540653
1240923082240923083CT27GENIChomozygous109540654
1240923932240923933GA11GENIChomozygous109540655
1240924137240924138AG5GENIChomozygous109540656
1240924889240924890TC16GENIChomozygous109540658
1240925684240925685AT18GENIChomozygous109540659
1240925879240925880AG4GENIChomozygous109540660
1240927723240927724AG22GENIChomozygous109540661
1240927781240927782GA18GENIChomozygous109540662
1240928880240928881AC8GENIChomozygous109540663
1240929944240929945CT19GENIChomozygous109540664
1240930182240930183AG22GENIChomozygous109540667
1240930959240930960AG18GENIChomozygous109540668
1240932476240932477AC22GENIChomozygous120684576
1240932473240932474AC23GENIChomozygous120684574