chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7113834036113834037AC17GENIChomozygous54228868
7113834739113834740GA12GENICpossibly homozygous54228870
7113836882113836883CT13GENIChomozygous54228872
7113837538113837539GA16GENIChomozygous54228874
7113841569113841570TTAGC3GENIChomozygous54228876
7113842425113842426CCCATTTCAAGAGT6GENIChomozygous54067363
7113845218113845219T-3GENIChomozygous54228878
7113845859113845860GA15GENICpossibly homozygous54228880
7113847218113847219A-2GENIChomozygous54228882
7113849674113849675CT6GENIChomozygous54228884
7113850620113850621AG27GENIChomozygous54067373
7113851006113851007GT26GENICpossibly homozygous54228886
7113853692113853693TA26GENIChomozygous54228891
7113857051113857052C-9GENICheterozygous54802201
7113859287113859288GGTTT1GENIChomozygous54228893
7113860455113860456A-16GENIChomozygous54067416
7113861910113861911AG26GENIChomozygous54228895
7113862643113862644G-5GENIChomozygous54067420
7113863738113863739GT4GENIChomozygous54228897
7113863739113863740CT4GENIChomozygous54228898
7113868446113868447CT17GENICpossibly homozygous54228900
7113868953113868954AC7GENICpossibly homozygous54067431
7113869847113869848TC29GENICpossibly homozygous54067432
7113870275113870276TG21GENIChomozygous54067434
7113870950113870951AT14GENICpossibly homozygous54067435
7113871094113871095TC9GENIChomozygous54067436
7113872900113872901C-6GENICheterozygous54067438
7113873692113873693AG3GENIChomozygous54067439
7113873773113873774CCTT4GENIChomozygous54067440
7113873804113873805GA5GENIChomozygous54228908
7113873816113873817AC6GENIChomozygous54228910
7113874102113874103AC31GENICpossibly homozygous54228914