chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1256786290256786291TC10GENIChomozygous108622719
1256786501256786502TC17GENIChomozygous108622720
1256786962256786963TC8GENIChomozygous120477110
1256786963256786964CT7GENIChomozygous120477111
1256787056256787057GA18GENIChomozygous108622722
1256787069256787070GA18GENIChomozygous108622723
1256787325256787326AG11GENIChomozygous108622724
1256787447256787448CA5GENIChomozygous120512679
1256787811256787812TC24GENIChomozygous108622726
1256787943256787944TC7GENIChomozygous108622727
1256788397256788398GA14GENIChomozygous108622728
1256788624256788625AC27GENIChomozygous108622729
1256789171256789172AG22GENIChomozygous108622730
1256790225256790226TC16GENIChomozygous108622733
1256790589256790590AT13GENIChomozygous108622735
1256790853256790854GC16GENIChomozygous108622736
1256791059256791060CT18GENIChomozygous108622737
1256791159256791160GA27GENIChomozygous108622738
1256792775256792776CT16GENIChomozygous108622740
1256793007256793008CT22GENIChomozygous108622741
1256793115256793116AG25GENIChomozygous108622742
1256795179256795180GT20GENIChomozygous108622743
1256795188256795189TG18GENIChomozygous108622744
1256798233256798234GC18GENIChomozygous108622746
1256798324256798325AC16GENIChomozygous108622747
1256798525256798526GA15GENIChomozygous108622748
1256799149256799150TA4GENIChomozygous108622749
1256799326256799327CT10GENIChomozygous108622750
1256800269256800270CT25GENIChomozygous108622751
1256800388256800389CT5GENIChomozygous108622752
1256800610256800611TC18GENIChomozygous108622753
1256801088256801089CT7GENIChomozygous108622754
1256802177256802178CT25GENIChomozygous108622755
1256802206256802207GA31GENIChomozygous108622756
1256802492256802493TC17GENIChomozygous108622757
1256802604256802605AG15GENIChomozygous108622758
1256803412256803413CT21GENIChomozygous108622759
1256803527256803528GA8GENIChomozygous108622760