chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2045782214578222CT6GENIChomozygous109233522
2045817894581790CT10GENIChomozygous109233526
2045822884582289CT11GENIChomozygous109296134
2045824004582401GA10GENIChomozygous109296136
2045826244582625CT8GENIChomozygous109233527
2045828304582831GA15GENIChomozygous109074767
2045829094582910TA16GENIChomozygous109233528
2045829564582957GT17GENICpossibly homozygous109074769
2045829954582996GA15GENIChomozygous109074771
2045830484583049CT11GENIChomozygous109233529
2045832574583258CT10GENIChomozygous109074773
2045832604583261TC11GENIChomozygous109233530
2045835624583563GT12GENIChomozygous109074777
2045835994583600GA12GENIChomozygous109296138
2045848804584881CT10GENIChomozygous109296140
2045859464585947AG14GENIChomozygous109296142
2045863384586339GA18GENIChomozygous109074781
2045865354586536TA18GENIChomozygous109074783
2045867244586725AG15GENIChomozygous109074789
2045868224586823GA12GENIChomozygous109296144
2045868774586878CT10GENIChomozygous109296146
2045877364587737TG5GENIChomozygous109296148
2045887474588748CT29GENICpossibly homozygous109296150
2045890254589026GA28GENIChomozygous109074793
2045893664589367CT18GENIChomozygous109296152
2045894224589423TC12GENIChomozygous109074797
2045902444590245GA12GENIChomozygous109296154
2045924614592462GT20GENIChomozygous109296156