chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
95088499250884993CA18GENIChomozygous117540750
95088516750885168AG21GENIChomozygous117540752
95088684150886842TC6GENIChomozygous117540754
95088727550887276CT14GENIChomozygous120337828
95089048450890485TC17GENIChomozygous117540756
95089054450890545AG15GENIChomozygous117540758
95089061350890614CT17GENIChomozygous117540760
95089182350891824TC19GENIChomozygous117540762
95089312850893129GC19GENIChomozygous117540764
95089375950893760AG17GENIChomozygous117540766
95089590350895904CG10GENIChomozygous126591824
95089706550897066AT18GENIChomozygous117540770
95089839850898399CT12GENIChomozygous117540772
95090057050900571AG5GENIChomozygous117335192
95090213850902139TG24GENIChomozygous117540776
95090307250903073GT16GENIChomozygous117540780
95090318350903184TG5GENIChomozygous117540782
95090546350905464TC16GENIChomozygous117540784
95090708050907081CT9GENIChomozygous120337830
95090755350907554GT10GENIChomozygous117335200
95090768150907682GA21GENIChomozygous120337831
95090840650908407CT5GENIChomozygous120337832
95091135350911354GA10GENIChomozygous120337833
95091630750916308GA7GENIChomozygous117540792
95091646350916464AG10GENIChomozygous117335208
95091708550917086AG13GENIChomozygous117540794
95091798850917989AC11GENIChomozygous120337834
95091891050918911AG19GENIChomozygous117540796
95092110350921104AC5GENIChomozygous120337835