chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1240908883240908884TC4GENIChomozygous108591006
1240909893240909894TG11GENIChomozygous109540634
1240910286240910287CT47GENIChomozygous109540635
1240910304240910305GA46GENIChomozygous109540636
1240911972240911973TC26GENIChomozygous109540637
1240912909240912910AT7GENICpossibly homozygous120782091
1240912910240912911TC6GENICheterozygous120782092
1240912945240912946AT11GENIChomozygous109540638
1240913993240913994AG34GENIChomozygous109540639
1240914672240914673TC32GENIChomozygous109540640
1240914673240914674GA31GENIChomozygous109540641
1240914891240914892GT28GENIChomozygous109540642
1240916187240916188TC41GENIChomozygous109540643
1240916222240916223TC37GENIChomozygous109540644
1240917229240917230CT36GENIChomozygous109540645
1240921982240921983CT11GENIChomozygous109540650
1240922514240922515CA41GENIChomozygous109540651
1240922777240922778GC34GENIChomozygous109540652
1240923082240923083CT26GENIChomozygous109540654
1240923932240923933GA20GENIChomozygous109540655
1240924137240924138AG15GENIChomozygous109540656
1240924889240924890TC20GENIChomozygous109540658
1240925684240925685AT17GENIChomozygous109540659
1240925879240925880AG8GENIChomozygous109540660
1240927723240927724AG39GENICpossibly homozygous109540661
1240927781240927782GA29GENIChomozygous109540662
1240929944240929945CT44GENIChomozygous109540664
1240930182240930183AG29GENIChomozygous109540667
1240930959240930960AG16GENIChomozygous109540668
1240932473240932474AC28GENIChomozygous120684574
1240932476240932477AC28GENIChomozygous120684576