chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
92332629423326294TTTTG21GENIChomozygous128689829
92332722723327228TA23GENIChomozygous117286197
92332728323327284GA24GENIChomozygous117286198
92332751823327519CT21GENIChomozygous117286199
92333157223331572GT26GENIChomozygous128689830
92333160823331609TA28GENIChomozygous117286200
92333291723332918CT16GENIChomozygous117286201
92333505823335059C13GENIChomozygous128689831
92333506023335071TTCTTTTTTCC14GENIChomozygous128689832
92333656123336562AG20GENIChomozygous117286202
92333711823337119CA11GENIChomozygous117286203
92333716423337165AG16GENIChomozygous117286204
92333886123338877AGATGGTCCTGACAGT22GENIChomozygous128689833
92333936223339363AC30GENIChomozygous117286205
92334093223340933GT26GENIChomozygous117286206
92334111923341120TC17GENIChomozygous117286207
92334119323341193A14GENIChomozygous128689834
92334122323341224CT17GENIChomozygous117286208
92334125723341258AC17GENIChomozygous117286209
92334126023341261AG17GENIChomozygous117286210
92334222923342230TC22GENIChomozygous117286211
92334536623345367TC36GENIChomozygous117286212
92334727023347271AC16GENIChomozygous117286213
92334908423349084A25GENIChomozygous128689835
92334945523349456GA22GENIChomozygous117286214
92335096823350969GC15GENIChomozygous117286215
92335142723351428TG19GENIChomozygous117286216
92335169923351700TC17GENIChomozygous117286217