chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
75328787053287871AG15GENIChomozygous53924937
75328803353288034TC19GENICpossibly homozygous53924939
75329103653291037AG19GENICpossibly homozygous54653028
75329106953291070TC24GENICpossibly homozygous54653030
75329479253294793GA7GENIChomozygous54653034
75329593453295935AG11GENIChomozygous53924944
75329678353296784GA14GENICheterozygous54653036
75329863453298635TC4GENICheterozygous54653038
75329888253298883GA10GENIChomozygous54653040
75329914653299147CCAT3GENICheterozygous54653042
75329946853299469T-3GENIChomozygous54195694
75330189053301891GT15GENICpossibly homozygous54653044
75330214353302147AAAT----1GENIChomozygous54653046
75330420853304210TG--6GENICheterozygous53924949
75330426053304261GA10GENICpossibly homozygous54653048
75330643953306440T-2GENIChomozygous54195695
75330675353306754AC20GENICpossibly homozygous54653050
75331001953310020GA28GENIChomozygous53924952
75331184253311843CT18GENIChomozygous54653052
75331193753311938AG8GENICheterozygous54653054
75331274953312750CT21GENICpossibly homozygous54653056
75331327453313275CG8GENIChomozygous53924953
75331350753313508TTGC4GENICheterozygous53924957
75331538053315381CCA2GENIChomozygous54653058
75331615853316159AG23GENICpossibly homozygous53924958
75331757953317580T-1GENIChomozygous54653060
75331822053318221GT12GENICpossibly homozygous54653062
75331866753318668TA9GENIChomozygous53924960
75332215353322154GA6GENIChomozygous53924967
75332221953322220CT12GENIChomozygous53924969
75332223053322231GA9GENICpossibly homozygous53924971
75332236453322365GA12GENIChomozygous53924973
75332241153322412TA17GENIChomozygous53924975
75332259653322597GGTTTT1GENIChomozygous54902669
75332355653323557CA18GENICpossibly homozygous53924982
75332458753324588A-6GENICheterozygous53924983
75332483553324836GA11GENIChomozygous54653064
75332560753325608AG10GENICpossibly homozygous53924991
75332727053327271GA9GENIChomozygous54653066