chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
102739763227397633CT23GENIChomozygous116532872
102739798827397989GA22GENIChomozygous116924073
102739813927398140AT26GENIChomozygous116532876
102739819627398197GA20GENIChomozygous116532878
102739830627398307TC25GENIChomozygous116924075
102739844927398450AG17GENIChomozygous116924077
102739862427398625CT21GENIChomozygous116532880
102739869327398694GA25GENICpossibly homozygous116924079
102740037127400372GA23GENIChomozygous116924081
102740103027401031AT20GENIChomozygous116924083
102740133427401335TC28GENIChomozygous116532884
102740285627402857AG8GENIChomozygous116924085
102740327527403276GA12GENIChomozygous116532888
102740382327403824AG24GENIChomozygous116924087
102740412827404129AT20GENIChomozygous116532892
102740461127404612TA9GENIChomozygous116924089
102740495327404954GC19GENIChomozygous116532898
102740578427405785GC23GENIChomozygous116532900
102740585127405852TC21GENIChomozygous116532902
102740746827407469GA28GENIChomozygous116924093
102740751327407514GC21GENIChomozygous116924095
102740893427408935TA28GENIChomozygous116532910
102740621427406215AG27GENIChomozygous116532904
102740675627406757AT23GENIChomozygous116532906
102740817027408171AG16GENIChomozygous116532908
102741028027410281CT12GENIChomozygous116924097
102741076127410762TC24GENIChomozygous116532914
102741130227411303TA21GENIChomozygous116532918
102741137827411379TC38GENIChomozygous116532920