chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3154513902154513903CT4GENICheterozygous648139550
3154514251154514255CGGC----9GENIChomozygous755968104
3154514259154514260CT10GENIChomozygous648139551
3154514276154514277TG10GENIChomozygous648139552
3154514414154514415AAGTCT10GENIChomozygous755968106
3154515300154515301GA12GENIChomozygous648139553
3154515475154515476GA9GENIChomozygous648139554
3154515627154515628GA8GENIChomozygous648139555
3154515681154515682TA7GENIChomozygous648139556
3154515884154515885AG6GENIChomozygous648139557
3154516260154516261TC16GENIChomozygous648139558
3154516490154516491AT24GENIChomozygous648139559
3154516884154516885AG20GENIChomozygous648139560
3154516887154516888GA20GENIChomozygous648139561
3154517156154517157AG16GENIChomozygous648139562
3154517166154517167TG14GENIChomozygous648139563
3154517351154517352G-21GENIChomozygous755968108
3154517632154517633G-10GENIChomozygous755968109
3154517898154517899TC9GENIChomozygous648139564
3154518068154518069GA24GENIChomozygous648139565
3154518158154518159TTA25GENIChomozygous755968110
3154519184154519185CCCA2GENICheterozygous755968112
3154519630154519636TCCCTC------5GENIChomozygous755968113
3154519872154519873AC17GENIChomozygous648139566
3154519897154519899TT--15GENIChomozygous755968114
3154519985154519986AG21GENIChomozygous648139567
3154520058154520059TC21GENIChomozygous648139568
3154521686154521687CT13GENIChomozygous648139569
3154521914154521915TTAA12GENICheterozygous755968117
3154521915154521916A-12GENICpossibly homozygous755968116
3154522134154522135AG16GENIChomozygous648139570