chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
32822375128223752CG10GENICpossibly homozygous670150884
32822389628223897CT12GENICpossibly homozygous670150885
32822426128224265GGGG----4GENIChomozygous768651006
32822528728225288TC23GENIChomozygous670150886
32822571028225711CG2GENIChomozygous670150887
32822594028225941AG20GENICpossibly homozygous670150888
32822601428226015CT11GENICheterozygous670150889
32822616728226168AG5GENIChomozygous670150890
32822806428228065TC6GENICheterozygous670150891
32822833928228340CG20GENICpossibly homozygous670150892
32823045028230451GA14GENIChomozygous670150893
32823144828231450TC--4GENICheterozygous768651009
32823257428232575CT12GENICpossibly homozygous670150894
32823285628232857CT12GENICheterozygous670150895
32823292428232925AG3GENIChomozygous670150896
32823302928233030CT15GENICpossibly homozygous670150897
32823312628233127CT21GENIChomozygous670150898
32823338828233389AAG2GENICheterozygous768651010
32823339128233392GGCAACTTCTACTAGAGC2GENICheterozygous768651011
32823341828233419CT8GENICheterozygous670150899
32823361328233614CG20GENICpossibly homozygous670150900
32823379228233793TC5GENIChomozygous670150901
32823379828233799CT9GENIChomozygous670150902
32823429428234295TTGG7GENICpossibly homozygous768651012
32823493928234940GGGA7GENIChomozygous768651013
32823529328235294CT9GENIChomozygous670150903
32823532728235328CT13GENICpossibly homozygous670150904
32823545928235460TC3GENICheterozygous670150905
32823553628235537TC3GENIChomozygous670150906
32823554828235549CA6GENIChomozygous670150907
32823569028235691CT10GENIChomozygous670150908
32823593828235939CA9GENIChomozygous670150909
32823655428236555GA15GENICpossibly homozygous670150910
32823728128237282GA15GENICpossibly homozygous670150911
32823802128238022AG11GENICheterozygous670150912
32823811328238114GC12GENIChomozygous670150913
32824019128240193GG--9GENICheterozygous768651015
32824060028240604ACTT----2GENIChomozygous768651016
32824180128241813TAGGTAGGTAGG------------1GENIChomozygous768651017