chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1675084107508411CA21GENIChomozygous47719493
1675103107510311AAAAAAC16GENIChomozygous47719497
1675105057510506CT10GENIChomozygous47719499
1675105657510566GT18GENIChomozygous47719501
1675109487510949TC12GENIChomozygous47719503
1675110907511091CCT16GENICheterozygous47920410
1675110917511092T-16GENICheterozygous47920412
1675113747511375CCA29GENIChomozygous47719505
1675136607513661AG12GENIChomozygous47719507
1675138987513901TTT---8GENIChomozygous47719509
1675139157513916CCTT12GENIChomozygous47719512
1675141797514180GA19GENIChomozygous47257691
1675174047517405GGA6GENIChomozygous47257708
1675174947517495AG11GENIChomozygous47719534
1675182347518235GC24GENIChomozygous47257711
1675193687519369AAACACACACACAC3GENICheterozygous47920416
1675200577520058A-10GENICpossibly homozygous47719538
1675210337521034AG18GENIChomozygous47719540
1675211017521102TC22GENIChomozygous47257724
1675218617521862GT26GENIChomozygous47257727
1675233017523302AC17GENIChomozygous47257728
1675097097509731GTGTGTGTGTGTGTGTGTGTGT----------------------5GENICheterozygous47941507
1675097117509731GTGTGTGTGTGTGTGTGTGT--------------------5GENICheterozygous47941508
1675104667510492GCCCCTTCACCCCTACCCACAGAGCT--------------------------11GENICheterozygous47941509
1675193687519369AAACACACACAC3GENICheterozygous47941510