chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
151859629518596296AG16GENIChomozygous139680786
151859636718596367AGTCCTT16GENIChomozygous139621236
151859725618597257A26GENICheterozygous139621237
151859728418597285CT27GENICheterozygous139680788
151859728618597287CT27GENICheterozygous139680789
151859730318597304GA28GENICheterozygous139680790
151859730418597305CT27GENICheterozygous139680791
151859733518597336GT25GENICheterozygous139680792
151859735218597353TA28GENICheterozygous139680793
151859743918597440CT20GENICheterozygous139680794
151859744018597441AG20GENICheterozygous139680795
151859744318597444GA20GENICheterozygous139680796
151859744818597449TC20GENICheterozygous139680797
151859670618596710ACTC19GENIChomozygous143603659
151859727518597276A27GENICheterozygous139621238
151859735918597359TT25GENICheterozygous139621239
151859738918597389G26GENICheterozygous139621240
151859742018597420ATAAAGCCTT20GENICheterozygous139621241
151859742718597431CAAG19GENICheterozygous139621242
151860419118604191A13GENICheterozygous143603660
151860451718604518CT18GENICheterozygous139680813
151860451818604519CT18GENICheterozygous139680814
151860452718604528GA18GENICheterozygous139680815
151860453118604532GA18GENICheterozygous139680816
151860453218604533GA18GENICheterozygous139680817
151860454618604547CT22GENICheterozygous139680818
151860455218604553C22GENICheterozygous139621245
151860456118604562AG22GENICheterozygous139680819
151860457418604575CT20GENICheterozygous139680820
151860457718604578GA21GENICheterozygous139680821
151860458018604580A21GENICheterozygous139621246
151860459918604600AG20GENICheterozygous139680822
151860460818604609CA22GENICheterozygous139680823
151860461918604620GA24GENICheterozygous139680824
151860462618604627CT25GENICheterozygous139680825
151860464118604642AT25GENICheterozygous139680826
151860464918604650CT22GENICheterozygous139680827
151860465018604651AG22GENICheterozygous139680828
151860465618604657CT21GENICheterozygous139680829